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Wyszukujesz frazę ""Corona‐Rivera, Alfredo"" wg kryterium: Autor


Tytuł :
Physiological concentrations of short-chain fatty acids induce the formation of neutrophil extracellular traps in vitro
Autorzy :
Íñiguez-Gutiérrez, Liliana
Godínez-Méndez, Lucila A
Fafutis-Morris, Mary
Padilla-Arellano, Jorge R
Corona-Rivera, Alfredo
Bueno-Topete, Miriam Ruth
Rojas-Rejón, Óscar A
Delgado-Rizo, Vidal
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Źródło :
International Journal of Immunopathology and Pharmacology; October 2020, Vol. 34 Issue: 1
Periodyk
Tytuł :
Hepatoblastoma in a patient with Goldenhar syndrome born to a diabetic motherHow to cite this article: CoronaRivera JR, Sánchez‐Zubieta F, Silva‐Padilla N, González‐Ramella O, López‐Marure E, Vélez‐Gómez E, Orozco‐Pérez J, Soto‐Chávez V, CoronaRivera A. 2006. Hepatoblastoma in a patient with Goldenhar syndrome born to a diabetic mother. Am J Med Genet Part A 140A:2834–2837.
Autorzy :
CoronaRivera, J. Román
Sánchez‐Zubieta, Fernando
Silva‐Padilla, Noemí
González‐Ramella, Oscar
López‐Marure, Eloy
Vélez‐Gómez, Ezequiel
Orozco‐Pérez, Jaime
Soto‐Chávez, Verónica
CoronaRivera, Alfredo
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Źródło :
American Journal of Medical Genetics. Part A; December 2006, Vol. 140 Issue: 24 p2834-2837, 4p
Periodyk
Tytuł :
Sydney crease frequency changes among the newborns and infantsHow to cite this article: CoronaRivera JR, Zarate‐Ramírez S, Pérez‐Molina JJ, CoronaRivera A. 2007. Sydney crease frequency changes among the newborns and infants. Am J Med Genet Part A 143A:387–389.
Autorzy :
CoronaRivera, J. Román
Zarate‐Ramírez, Soledad
Pérez‐Molina, J. Jesús
CoronaRivera, Alfredo
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Źródło :
American Journal of Medical Genetics. Part A; February 2007, Vol. 143 Issue: 4 p387-389, 3p
Periodyk
Tytuł :
MTHFR C677T and A1298C variants in Mexican Mestizo infants with neural tube defects from Western Mexico.
Autorzy :
Aranda-Sánchez CI; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca', Civil Hospital of Guadalajara, Guadalajara, Mexico.
Bobadilla-Morales L; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca', Civil Hospital of Guadalajara, Guadalajara, Mexico.; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
Corona-Rivera A; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca', Civil Hospital of Guadalajara, Guadalajara, Mexico.; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
Cuero-Quezada I; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
Santana-Hernández J; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
Baldomero-López A; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca', Civil Hospital of Guadalajara, Guadalajara, Mexico.
Romero-Bolaño YM; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca', Civil Hospital of Guadalajara, Guadalajara, Mexico.
Peña-Padilla C; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca', Civil Hospital of Guadalajara, Guadalajara, Mexico.
Corona-Rivera JR; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca', Civil Hospital of Guadalajara, Guadalajara, Mexico.; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
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Źródło :
Congenital anomalies [Congenit Anom (Kyoto)] 2021 Sep; Vol. 61 (5), pp. 188-192. Date of Electronic Publication: 2021 May 29.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
[Prader-Willi and Angelman syndromes: case series diagnosed by MS-MLPA assay].
Autorzy :
Rios-Flores IM; Hospital Civil de Guadalajara 'Dr. Juan I. Menchaca', División de Pediatría, Servicio de Genética. Guadalajara, Jalisco, México.
Bobadilla-Morales L; Hospital Civil de Guadalajara 'Dr. Juan I. Menchaca', División de Auxiliares de Diagnóstico y Paramédicos, Unidad de Citogenética. Guadalajara, Jalisco, México.
Peña Padilla C; Hospital Civil de Guadalajara 'Dr. Juan I. Menchaca', División de Pediatría, Servicio de Genética. Guadalajara, Jalisco, México.
Corona-Rivera A; Hospital Civil de Guadalajara 'Dr. Juan I. Menchaca', División de Auxiliares de Diagnóstico y Paramédicos, Unidad de Citogenética. Guadalajara, Jalisco, México.
Acosta-Fernández E; Hospital Civil de Guadalajara 'Dr. Juan I. Menchaca', División de Pediatría, Servicio de Genética. Guadalajara, Jalisco, México.
Santana-Hernández J; Hospital Civil de Guadalajara 'Dr. Juan I. Menchaca', División de Auxiliares de Diagnóstico y Paramédicos, Unidad de Citogenética. Guadalajara, Jalisco, México.
Brukman-Jiménez SA; Hospital Civil de Guadalajara 'Dr. Juan I. Menchaca', División de Auxiliares de Diagnóstico y Paramédicos, Unidad de Citogenética. Guadalajara, Jalisco, México.
Corona Rivera JR; Universidad de Guadalajara, Centro Universitario de Ciencias de la Salud, Departamento de Biología Molecular y Genómica, Instituto de Genética Humana 'Dr. Enrique Corona Rivera'. Guadalajara, Jalisco, México.
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Transliterated Title :
Síndromes Prader-Willi y Angelman: serie de casos diagnosticados mediante la técnica de MS-MLPA.
Źródło :
Revista medica del Instituto Mexicano del Seguro Social [Rev Med Inst Mex Seguro Soc] 2021 Jun 14; Vol. 59 (2), pp. 170-178. Date of Electronic Publication: 2021 Jun 14.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Angelman Syndrome*/diagnosis
Angelman Syndrome*/genetics
Prader-Willi Syndrome*/diagnosis
Prader-Willi Syndrome*/genetics
DNA Methylation ; Humans ; Infant, Newborn ; Uniparental Disomy
Czasopismo naukowe
Tytuł :
Prevalence of open neural tube defects and risk factors related to isolated anencephaly and spina bifida in live births from the "Dr. Juan I. Menchaca" Civil Hospital of Guadalajara (Jalisco, Mexico).
Autorzy :
Corona-Rivera JR; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
Olvera-Molina S; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Pérez-Molina JJ; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Aranda-Sánchez CI; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Bobadilla-Morales L; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
Corona-Rivera A; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
Peña-Padilla C; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Ruiz-Gómez A; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Morales-Domínguez GE; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
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Źródło :
Congenital anomalies [Congenit Anom (Kyoto)] 2021 Mar; Vol. 61 (2), pp. 46-54. Date of Electronic Publication: 2020 Nov 05.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Family history of thyroid disease and risk of congenital hypothyroidism in neonates with Down síndrome.
Autorzy :
Corona-Rivera JR; Department of Genetics and Cytogenetics Unit, Pediatrics Division, Congenital Anomalies Registration and Research Center, Hospital Civil de Guadalajara 'Dr. Juan I. Menchaca'.; Department of Molecular Biology and Genomics, Health Sciences University Center, Instituto de Genética Humana 'Dr. Enrique Corona-Rivera', Universidad de Guadalajara.
Andrade-Romo TO; Department of Genetics and Cytogenetics Unit, Pediatrics Division, Congenital Anomalies Registration and Research Center, Hospital Civil de Guadalajara 'Dr. Juan I. Menchaca'.
Aguirre-Salas LM; Endocrinology Department, Pediatrics Division, Hospital Civil de Guadalajara 'Dr. Juan I. Menchaca'.
Bobadilla-Morales L; Department of Genetics and Cytogenetics Unit, Pediatrics Division, Congenital Anomalies Registration and Research Center, Hospital Civil de Guadalajara 'Dr. Juan I. Menchaca'.; Department of Molecular Biology and Genomics, Health Sciences University Center, Instituto de Genética Humana 'Dr. Enrique Corona-Rivera', Universidad de Guadalajara.
Aranda-Sánchez CI; Department of Genetics and Cytogenetics Unit, Pediatrics Division, Congenital Anomalies Registration and Research Center, Hospital Civil de Guadalajara 'Dr. Juan I. Menchaca'.
Corona-Rivera A; Department of Genetics and Cytogenetics Unit, Pediatrics Division, Congenital Anomalies Registration and Research Center, Hospital Civil de Guadalajara 'Dr. Juan I. Menchaca'.; Department of Molecular Biology and Genomics, Health Sciences University Center, Instituto de Genética Humana 'Dr. Enrique Corona-Rivera', Universidad de Guadalajara.
Pérez-Ramírez RO; Neonatology Department, Pediatrics Division, Hospital Civil de Guadalajara 'Dr. Juan I. Menchaca'. Guadalajara, Jalisco, Mexico.
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Transliterated Title :
Historia familiar de enfermedad tiroidea y riesgo de hipotiroidismo congénito en neonatos con síndrome de Down.
Źródło :
Gaceta medica de Mexico [Gac Med Mex] 2021; Vol. 157 (2), pp. 133-139.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Complete blood count differences in a cohort of Down syndrome neonates with transient abnormal myelopoiesis screened for GATA1 pathogenic variants.
Autorzy :
Orozco-Vela M; University of Guadalajara, Health Sciences University Center, Department of Molecular Biology and Genomics, 'Dr. Enrique Corona Rivera' Institute of Human Genetics, Guadalajara, Jalisco, Mexico.
Corona-Rivera A; University of Guadalajara, Health Sciences University Center, Department of Molecular Biology and Genomics, 'Dr. Enrique Corona Rivera' Institute of Human Genetics, Guadalajara, Jalisco, Mexico.; 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Division of Pediatrics and Paramedic and Auxiliary Diagnostic Services, Service of Hematology-Oncology, Cytogenetics Unit, Guadalajara, Jalisco, Mexico.
Cruz-Osorio RM; 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Division of Pediatrics and Paramedic and Auxiliary Diagnostic Services, Service of Hematology-Oncology, Cytogenetics Unit, Guadalajara, Jalisco, Mexico.
Mendoza-Maldonado L; 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Division of Pediatrics and Paramedic and Auxiliary Diagnostic Services, Service of Hematology-Oncology, Cytogenetics Unit, Guadalajara, Jalisco, Mexico.
Márquez-Mora A; 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Division of Pediatrics and Paramedic and Auxiliary Diagnostic Services, Service of Hematology-Oncology, Cytogenetics Unit, Guadalajara, Jalisco, Mexico.
Barba-Barba CC; 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Division of Pediatrics and Paramedic and Auxiliary Diagnostic Services, Service of Hematology-Oncology, Cytogenetics Unit, Guadalajara, Jalisco, Mexico.
Peña-Padilla C; 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Division of Pediatrics, Service of Genetics, Center for Registry and Research on Congenital Anomalies (CRIAC), Guadalajara, Jalisco, Mexico.
Baldomero-López A; 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Division of Pediatrics, Service of Genetics, Center for Registry and Research on Congenital Anomalies (CRIAC), Guadalajara, Jalisco, Mexico.
Bobadilla-Morales L; University of Guadalajara, Health Sciences University Center, Department of Molecular Biology and Genomics, 'Dr. Enrique Corona Rivera' Institute of Human Genetics, Guadalajara, Jalisco, Mexico.; 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Division of Pediatrics and Paramedic and Auxiliary Diagnostic Services, Service of Hematology-Oncology, Cytogenetics Unit, Guadalajara, Jalisco, Mexico.
Corona-Rivera JR; University of Guadalajara, Health Sciences University Center, Department of Molecular Biology and Genomics, 'Dr. Enrique Corona Rivera' Institute of Human Genetics, Guadalajara, Jalisco, Mexico.; 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Division of Pediatrics, Service of Genetics, Center for Registry and Research on Congenital Anomalies (CRIAC), Guadalajara, Jalisco, Mexico.
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Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2020 Sep; Vol. 182 (9), pp. 2085-2093. Date of Electronic Publication: 2020 Jul 18.
Typ publikacji :
Journal Article
MeSH Terms :
Down Syndrome/*blood
GATA1 Transcription Factor/*genetics
Leukemoid Reaction/*blood
Adult ; Blood Cell Count ; Down Syndrome/genetics ; Down Syndrome/pathology ; Female ; Humans ; Infant ; Infant, Newborn ; Leukemoid Reaction/genetics ; Leukemoid Reaction/pathology ; Male ; Middle Aged ; Mutation/genetics
SCR Disease Name :
Myeloproliferative Syndrome, Transient
Czasopismo naukowe
Tytuł :
Acute liver failure in a male patient with NGLY1-congenital disorder of deglycosylation.
Autorzy :
Rios-Flores IM; Service of Genetics and Cytogenetics Unit, Division of Pediatrics, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Mexico.
Bonal-Pérez MÁ; Pediatric Intensive Care Unit, Real San Jose Hospital, Zapopan, Mexico.
Castellanos-González A; Pediatric Neurology Consultant, Real San Jose Hospital, Zapopan, Mexico.
Velez-Gómez E; Service of Pathology, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Mexico.
Bertoli-Avella AM; Centogene AG, Rostock, Germany.
Bobadilla-Morales L; Service of Genetics and Cytogenetics Unit, Division of Pediatrics, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Mexico; University of Guadalajara, Health Sciences University Center, Department of Molecular Biology and Genomics, 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Guadalajara, Jalisco, Mexico.
Peña-Padilla C; Service of Genetics and Cytogenetics Unit, Division of Pediatrics, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Mexico.
Appendini-Andrade V; Service of Genetics and Cytogenetics Unit, Division of Pediatrics, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Mexico.
Corona-Rivera A; Service of Genetics and Cytogenetics Unit, Division of Pediatrics, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Mexico; University of Guadalajara, Health Sciences University Center, Department of Molecular Biology and Genomics, 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Guadalajara, Jalisco, Mexico.
Romero-Valenzuela I; Service of Genetics and Cytogenetics Unit, Division of Pediatrics, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Mexico.
Corona-Rivera JR; Service of Genetics and Cytogenetics Unit, Division of Pediatrics, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Mexico; University of Guadalajara, Health Sciences University Center, Department of Molecular Biology and Genomics, 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Guadalajara, Jalisco, Mexico. Electronic address: .
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Źródło :
European journal of medical genetics [Eur J Med Genet] 2020 Aug; Vol. 63 (8), pp. 103952. Date of Electronic Publication: 2020 May 15.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Congenital Disorders of Glycosylation/*pathology
Liver Failure, Acute/*etiology
Peptide-N4-(N-acetyl-beta-glucosaminyl) Asparagine Amidase/*genetics
Child, Preschool ; Congenital Disorders of Glycosylation/complications ; Congenital Disorders of Glycosylation/genetics ; Humans ; Liver/pathology ; Liver Failure, Acute/pathology ; Male ; Mutation
Czasopismo naukowe
Tytuł :
Extracranial midline defects in a patient with craniofrontonasal syndrome with a novel EFNB1 mutation.
Autorzy :
Acosta-Fernández E; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Zenteno JC; Department of Genetics, Institute of Ophthalmology 'Conde de Valenciana', Mexico City, Mexico.; Faculty of Medicine, Department of Biochemistry, UNAM, Mexico City, Mexico.
Chacón-Camacho OF; Department of Genetics, Institute of Ophthalmology 'Conde de Valenciana', Mexico City, Mexico.; School of Medicine, Faculty of Superior Studies-Iztacala, UNAM, Tlalnepantla, Mexico.
Peña-Padilla C; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Bobadilla-Morales L; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.; University of Guadalajara Health Sciences University Center, Department of Molecular Biology and Genomics, 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Guadalajara, Mexico.
Corona-Rivera A; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.; University of Guadalajara Health Sciences University Center, Department of Molecular Biology and Genomics, 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Guadalajara, Mexico.
Romo-Huerta CO; Service of Ophthalmology, Division of Pediatrics, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Zepeda-Romero LC; Service of Neonatal Ophthalmology, Division of Pediatrics, 'Fray Antonio Alcalde' Civil Hospital of Guadalajara, Guadalajara, Mexico.
López-Marure E; Service of Radiology, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Acosta-León J; Service of Urology, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
García-Cruz D; University of Guadalajara Health Sciences University Center, Department of Molecular Biology and Genomics, 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Guadalajara, Mexico.
Maciel-Cruz EJ; University of Guadalajara Health Sciences University Center, Department of Molecular Biology and Genomics, 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Guadalajara, Mexico.
Corona-Rivera JR; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.; University of Guadalajara Health Sciences University Center, Department of Molecular Biology and Genomics, 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Guadalajara, Mexico.
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Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2020 May; Vol. 182 (5), pp. 1223-1229. Date of Electronic Publication: 2020 Feb 05.
Typ publikacji :
Case Reports
MeSH Terms :
Agenesis of Corpus Callosum/*genetics
Craniofacial Abnormalities/*genetics
Ephrin-B1/*genetics
Hernias, Diaphragmatic, Congenital/*genetics
Agenesis of Corpus Callosum/diagnostic imaging ; Agenesis of Corpus Callosum/pathology ; Child ; Child, Preschool ; Craniofacial Abnormalities/diagnostic imaging ; Craniofacial Abnormalities/pathology ; Exons/genetics ; Female ; Hernias, Diaphragmatic, Congenital/diagnostic imaging ; Hernias, Diaphragmatic, Congenital/pathology ; Heterozygote ; Humans ; Infant ; Male ; Mutation/genetics ; Skull/diagnostic imaging ; Skull/pathology
SCR Disease Name :
Craniofrontonasal dysplasia
Raport
Tytuł :
Ring chromosome 6 in a child with anterior segment dysgenesis and review of its overlap with other FOXC1 deletion phenotypes.
Autorzy :
Corona-Rivera JR; Center for Registry and Research on Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Division of Pediatrics, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
Corona-Rivera A; Center for Registry and Research on Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Division of Pediatrics, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
Zepeda-Romero LC; Service of Ophthalmology, Division of Pediatrics, 'Fray Antonio Alcalde' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Rios-Flores IM; Center for Registry and Research on Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Division of Pediatrics, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Rivera-Vargas J; Center for Registry and Research on Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Division of Pediatrics, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
Orozco-Vela M; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
Santana-Bejarano UF; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
Torres-Anguiano E; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
Pinto-Cardoso M; Department of Human Genetics, National Health Institute Doutor Ricardo Jorge, Lisbon, Portugal.
David D; Department of Human Genetics, National Health Institute Doutor Ricardo Jorge, Lisbon, Portugal.
Bobadilla-Morales L; Center for Registry and Research on Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Division of Pediatrics, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.; 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Mexico.
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Źródło :
Congenital anomalies [Congenit Anom (Kyoto)] 2019 Sep; Vol. 59 (5), pp. 174-178. Date of Electronic Publication: 2018 Oct 09.
Typ publikacji :
Case Reports; Journal Article; Review
MeSH Terms :
Gene Deletion*
Phenotype*
Chromosome Disorders/*diagnosis
Chromosome Disorders/*genetics
Eye Abnormalities/*diagnosis
Eye Abnormalities/*genetics
Forkhead Transcription Factors/*genetics
Chromosome Banding ; Chromosome Deletion ; Chromosomes, Human, Pair 6/genetics ; Female ; Humans ; Infant, Newborn ; Karyotype ; Male ; Ring Chromosomes ; Young Adult
SCR Disease Name :
Anterior segment mesenchymal dysgenesis; Chromosome 6 ring syndrome
Czasopismo naukowe
Tytuł :
Maternal risk factors for congenital heart defects in infants with Down syndrome from Western Mexico.
Autorzy :
Corona-Rivera JR; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico.
Nieto-García R; Service of Cardiology, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Gutiérrez-Chávez AS; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Bobadilla-Morales L; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico.
Rios-Flores IM; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Corona-Rivera A; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico.
Fabián-Morales GE; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Zavala-Cortés I; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Lugo-Iglesias C; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Peña-Padilla C; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
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Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2019 Sep; Vol. 179 (9), pp. 1857-1865. Date of Electronic Publication: 2019 Jul 19.
Typ publikacji :
Journal Article
MeSH Terms :
Down Syndrome/*epidemiology
Heart Defects, Congenital/*epidemiology
Heart Septal Defects/*epidemiology
Heart Septal Defects, Atrial/*epidemiology
Adult ; Down Syndrome/complications ; Down Syndrome/physiopathology ; Female ; Heart Defects, Congenital/complications ; Heart Defects, Congenital/physiopathology ; Heart Septal Defects/complications ; Heart Septal Defects/physiopathology ; Heart Septal Defects, Atrial/complications ; Heart Septal Defects, Atrial/physiopathology ; Humans ; Infant ; Male ; Maternal Age ; Mexico/epidemiology ; Paternal Age ; Pregnancy ; Risk Factors ; United States/epidemiology
SCR Disease Name :
Atrioventricular Septal Defect
Czasopismo naukowe
Tytuł :
In vitro effect of curcumin in combination with chemotherapy drugs in Ph acute lymphoblastic leukemia cells.
Autorzy :
Santana-Bejarano UF; Cytogenetics and Genomics Laboratory, Human Genetics Institute 'Dr. Enrique Corona Rivera', Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco 44340, México.; PhD Program in Molecular Biology and Human Genetics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco 44340, México.
Bobadilla-Morales L; Cytogenetics and Genomics Laboratory, Human Genetics Institute 'Dr. Enrique Corona Rivera', Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco 44340, México.; PhD Program in Molecular Biology and Human Genetics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco 44340, México.; Cytogenetics Unit, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco 44340, México.
Mendoza-Maldonado L; Cytogenetics and Genomics Laboratory, Human Genetics Institute 'Dr. Enrique Corona Rivera', Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco 44340, México.; PhD Program in Molecular Biology and Human Genetics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco 44340, México.
Torres-Anguiano E; Cytogenetics and Genomics Laboratory, Human Genetics Institute 'Dr. Enrique Corona Rivera', Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco 44340, México.; PhD Program in Molecular Biology and Human Genetics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco 44340, México.
Brukman-Jiménez SA; Cytogenetics and Genomics Laboratory, Human Genetics Institute 'Dr. Enrique Corona Rivera', Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco 44340, México.; PhD Program in Molecular Biology and Human Genetics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco 44340, México.
Barba-Barba CC; Cytogenetics Unit, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco 44340, México.
Corona-Rivera JR; Cytogenetics and Genomics Laboratory, Human Genetics Institute 'Dr. Enrique Corona Rivera', Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco 44340, México.; PhD Program in Molecular Biology and Human Genetics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco 44340, México.
Corona-Rivera A; Cytogenetics and Genomics Laboratory, Human Genetics Institute 'Dr. Enrique Corona Rivera', Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco 44340, México.; PhD Program in Molecular Biology and Human Genetics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco 44340, México.; Cytogenetics Unit, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco 44340, México.
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Źródło :
Oncology letters [Oncol Lett] 2019 Jun; Vol. 17 (6), pp. 5224-5240. Date of Electronic Publication: 2019 Apr 02.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Prevalence and risk factors for Down syndrome: A hospital-based single-center study in Western Mexico.
Autorzy :
Corona-Rivera JR; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico.
Martínez-Macías FJ; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Bobadilla-Morales L; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico.
Corona-Rivera A; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico.
Peña-Padilla C; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Rios-Flores IM; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Flores-Guevara PA; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Orozco-Vela M; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico.
Aranda-Sánchez CI; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetics Unit, Pediatrics Division, Dr. Juan I. Menchaca Civil Hospital of Guadalajara, Guadalajara, Jalisco, Mexico.
Brukman-Jiménez SA; Dr. Enrique Corona-Rivera Institute of Human Genetics, Department of Molecular Biology and Genomics, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco, Mexico.
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Źródło :
American journal of medical genetics. Part A [Am J Med Genet A] 2019 Mar; Vol. 179 (3), pp. 435-441. Date of Electronic Publication: 2019 Jan 21.
Typ publikacji :
Journal Article
MeSH Terms :
Down Syndrome/*epidemiology
Adolescent ; Adult ; Case-Control Studies ; Down Syndrome/etiology ; Female ; Humans ; Male ; Maternal Exposure/adverse effects ; Mexico/epidemiology ; Middle Aged ; Odds Ratio ; Pregnancy ; Prevalence ; Risk Assessment ; Risk Factors ; Young Adult
Czasopismo naukowe
Tytuł :
Prevalence of orofacial clefts and risks for nonsyndromic cleft lip with or without cleft palate in newborns at a university hospital from West Mexico.
Autorzy :
Corona-Rivera JR; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.; Department of Molecular Biology and Genomics, Health Sciences University Centre, 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, University of Guadalajara, Guadalajara, Mexico.
Bobadilla-Morales L; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.; Department of Molecular Biology and Genomics, Health Sciences University Centre, 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, University of Guadalajara, Guadalajara, Mexico.
Corona-Rivera A; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.; Department of Molecular Biology and Genomics, Health Sciences University Centre, 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, University of Guadalajara, Guadalajara, Mexico.
Peña-Padilla C; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Olvera-Molina S; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Orozco-Martín MA; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
García-Cruz D; Department of Molecular Biology and Genomics, Health Sciences University Centre, 'Dr. Enrique Corona-Rivera' Institute of Human Genetics, University of Guadalajara, Guadalajara, Mexico.
Ríos-Flores IM; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Gómez-Rodríguez BG; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Rivas-Soto G; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
Pérez-Molina JJ; Center for Registry and Research in Congenital Anomalies (CRIAC), Service of Genetics and Cytogenetic Unit, Pediatric Division, 'Dr. Juan I. Menchaca' Civil Hospital of Guadalajara, Guadalajara, Mexico.
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Źródło :
Congenital anomalies [Congenit Anom (Kyoto)] 2018 Jul; Vol. 58 (4), pp. 117-123. Date of Electronic Publication: 2018 Mar 04.
Typ publikacji :
Journal Article
MeSH Terms :
Cleft Lip/*epidemiology
Cleft Palate/*epidemiology
Adult ; Case-Control Studies ; Cleft Lip/classification ; Female ; Hospitals, University ; Humans ; Infant, Newborn ; Live Birth ; Male ; Mexico/epidemiology ; Mothers ; Pregnancy ; Prevalence ; Prospective Studies ; Risk Factors ; Young Adult
Czasopismo naukowe
Tytuł :
Expression profile of NF-κB regulated genes in sporadic colorectal cancer patients.
Autorzy :
González-Quezada BA; Cytogenetics and Genomics Laboratory, Human Genetic Institute 'Dr. Enrique Corona Rivera', University of Guadalajara, Guadalajara, Jalisco 44340, México.; Cytogenetics Unit, Pediatric Hematology and Oncology Service, Hospital Civil of Guadalajara 'Dr. Juan I. Menchaca', Guadalajara, Jalisco 44340, México.
Santana-Bejarano UF; Cytogenetics and Genomics Laboratory, Human Genetic Institute 'Dr. Enrique Corona Rivera', University of Guadalajara, Guadalajara, Jalisco 44340, México.; Cytogenetics Unit, Pediatric Hematology and Oncology Service, Hospital Civil of Guadalajara 'Dr. Juan I. Menchaca', Guadalajara, Jalisco 44340, México.
Corona-Rivera A; Cytogenetics and Genomics Laboratory, Human Genetic Institute 'Dr. Enrique Corona Rivera', University of Guadalajara, Guadalajara, Jalisco 44340, México.; Cytogenetics Unit, Pediatric Hematology and Oncology Service, Hospital Civil of Guadalajara 'Dr. Juan I. Menchaca', Guadalajara, Jalisco 44340, México.
Pimentel-Gutiérrez HJ; Cytogenetics and Genomics Laboratory, Human Genetic Institute 'Dr. Enrique Corona Rivera', University of Guadalajara, Guadalajara, Jalisco 44340, México.; Cytogenetics Unit, Pediatric Hematology and Oncology Service, Hospital Civil of Guadalajara 'Dr. Juan I. Menchaca', Guadalajara, Jalisco 44340, México.
Silva-Cruz R; Cytogenetics and Genomics Laboratory, Human Genetic Institute 'Dr. Enrique Corona Rivera', University of Guadalajara, Guadalajara, Jalisco 44340, México.
Ortega-De-la-Torre C; Cytogenetics Unit, Pediatric Hematology and Oncology Service, Hospital Civil of Guadalajara 'Dr. Juan I. Menchaca', Guadalajara, Jalisco 44340, México.
Franco-Topete R; Pathological Anatomy Service, Hospital Civil of Guadalajara 'Dr. Juan I. Menchaca', Guadalajara, Jalisco 44340, México.
Franco-Topete K; Pathological Anatomy Service, Hospital Civil of Guadalajara 'Dr. Juan I. Menchaca', Guadalajara, Jalisco 44340, México.
Centeno-Flores MW; Colon and Rectum Service, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco 44340, México.
Maciel-Gutiérrez VM; Colon and Rectum Service, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco 44340, México.
Corona-Rivera JR; Cytogenetics and Genomics Laboratory, Human Genetic Institute 'Dr. Enrique Corona Rivera', University of Guadalajara, Guadalajara, Jalisco 44340, México.
Armendáriz-Borunda J; Molecular Biology and Gene Therapy Institute, Health Sciences University Center, University of Guadalajara, Guadalajara, Jalisco 44340, México.
Bobadilla-Morales L; Cytogenetics and Genomics Laboratory, Human Genetic Institute 'Dr. Enrique Corona Rivera', University of Guadalajara, Guadalajara, Jalisco 44340, México.; Cytogenetics Unit, Pediatric Hematology and Oncology Service, Hospital Civil of Guadalajara 'Dr. Juan I. Menchaca', Guadalajara, Jalisco 44340, México.
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Źródło :
Oncology letters [Oncol Lett] 2018 May; Vol. 15 (5), pp. 7344-7354. Date of Electronic Publication: 2018 Mar 07.
Typ publikacji :
Journal Article
Czasopismo naukowe

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