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


Wyświetlanie 1-5 z 5
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 May 20. Date of Electronic Publication: 2021 May 20.
Typ publikacji :
Journal Article
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 :
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 :
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 :
Prevalence and risk factors for gastroschisis in a public hospital from west México.
Autorzy :
Robledo-Aceves M; 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
Mellín-Sánchez EL
Corona-Rivera A
Pérez-Molina JJ
Cárdenas-Ruiz Velasco JJ
Corona-Rivera JR
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Źródło :
Congenital anomalies [Congenit Anom (Kyoto)] 2015 May; Vol. 55 (2), pp. 73-80.
Typ publikacji :
Journal Article
MeSH Terms :
Hospitals, Public*
Gastroschisis/*epidemiology
Adolescent ; Adult ; Case-Control Studies ; Female ; Humans ; Infant ; Infant, Newborn ; Male ; Mexico/epidemiology ; Odds Ratio ; Pregnancy ; Prevalence ; Risk Factors ; Young Adult
Czasopismo naukowe
    Wyświetlanie 1-5 z 5

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