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Tytuł :
Preimplantation Genetic Screening and The Success Rate of In Vitro Fertilization: A Three-Years Study on Iranian Population.
Autorzy :
Totonchi M; Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.; Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
Babaabasi B; Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Najafi H; Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.; Departments of Genetics, Faculty of Biological Sciences, Tarbiat Modares University, Tehran, Iran.
Rezazadeh Valojerdi M; Department of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Eftekhari-Yazdi P; Department of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Karimian L; Department of Embryology, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Almadani N; Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Mohseni Meybodi A; Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Kimiai M; Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Mashayekhi M; Department of Endocrinology and Female Infertility, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Madani T; Department of Endocrinology and Female Infertility, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran.
Gourabi H; Department of Genetics, Reproductive Biomedicine Research Center, Royan Institute for Reproductive Biomedicine, ACECR, Tehran, Iran. Electronic Address:.; Department of Stem Cells and Developmental Biology, Cell Science Research Center, Royan Institute for Stem Cell Biology and Technology, ACECR, Tehran, Iran.
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Źródło :
Cell journal [Cell J] 2021 Jan; Vol. 22 (4), pp. 467-475. Date of Electronic Publication: 2020 Apr 22.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Complex chromosomal rearrangements of human chromosome 21 in a patient manifesting clinical features partially overlapped with that of Down syndrome.
Autorzy :
Imaizumi T; Institute of Medical Genetics, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ward, Tokyo, 162-8666, Japan.; Department of Pediatrics, St. Marianna University School of Medicine, Kawasaki, Japan.
Yamamoto-Shimojima K; Institute of Medical Genetics, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ward, Tokyo, 162-8666, Japan.; Japan Society for the Promotion of Science (RPD), Tokyo, Japan.; Department of Transfusion Medicine and Cell Processing, Tokyo Women's Medical University, Tokyo, Japan.; Tokyo Women's Medical University Institute for Integrated Medical Sciences, Tokyo, Japan.
Yanagishita T; Institute of Medical Genetics, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ward, Tokyo, 162-8666, Japan.; Department of Pediatrics, Tokyo Women's Medical University, Tokyo, Japan.
Ondo Y; Institute of Medical Genetics, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ward, Tokyo, 162-8666, Japan.
Nishi E; Department of Medical Genetics, Osaka Women's and Children's Hospital, Osaka, Japan.
Okamoto N; Department of Medical Genetics, Osaka Women's and Children's Hospital, Osaka, Japan.
Yamamoto T; Institute of Medical Genetics, Tokyo Women's Medical University, 8-1 Kawada-cho, Shinjuku-ward, Tokyo, 162-8666, Japan. .; Department of Pediatrics, St. Marianna University School of Medicine, Kawasaki, Japan. .; Tokyo Women's Medical University Institute for Integrated Medical Sciences, Tokyo, Japan. .; Department of Pediatrics, Tokyo Women's Medical University, Tokyo, Japan. .
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Źródło :
Human genetics [Hum Genet] 2020 Dec; Vol. 139 (12), pp. 1555-1563. Date of Electronic Publication: 2020 Jun 13.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Chromosomes, Human/*genetics
Chromosomes, Human, Pair 21/*genetics
Down Syndrome/*genetics
Adaptor Proteins, Vesicular Transport/genetics ; Chromosome Aberrations ; Comparative Genomic Hybridization/methods ; Core Binding Factor Alpha 2 Subunit/genetics ; DNA-Binding Proteins/genetics ; Down Syndrome/physiopathology ; Female ; Gene Dosage/genetics ; Genetic Association Studies ; Humans ; In Situ Hybridization, Fluorescence/methods ; Infant ; Microarray Analysis/methods ; Minor Histocompatibility Antigens/genetics ; Muscle Proteins/genetics ; Superoxide Dismutase-1/genetics ; Whole Genome Sequencing
SCR Disease Name :
Down Syndrome Critical Region
Czasopismo naukowe
Tytuł :
Evolution of the parthenogenetic rock lizard hybrid karyotype: Robertsonian translocation between two maternal chromosomes in Darevskia rostombekowi.
Autorzy :
Spangenberg V; Vavilov Institute of General Genetics, RAS, Gubkin 3, Moscow, 119991, Russia. .
Kolomiets O; Vavilov Institute of General Genetics, RAS, Gubkin 3, Moscow, 119991, Russia.
Stepanyan I; Scientific Center of Zoology and Hydroecology, Yerevan, Armenia.
Galoyan E; Severtsov Institute of Ecology and Evolution, RAS, Moscow, Russia.
de Bello Cioffi M; Laboratório de Citogenética de Peixes, Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos, SP, Brazil.; Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Jena, Germany.
Martynova E; Skolkovo Institute of Science and Technology, Moscow, Russia.
Martirosyan I; Institute of Gene Biology, RAS, Moscow, Russia.
Grishaeva T; Vavilov Institute of General Genetics, RAS, Gubkin 3, Moscow, 119991, Russia.
Danielyan F; Department of Zoology, Yerevan State University, Yerevan, Armenia.
Al-Rikabi A; Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Jena, Germany.
Liehr T; Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Jena, Germany.
Arakelyan M; Department of Zoology, Yerevan State University, Yerevan, Armenia.
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Źródło :
Chromosoma [Chromosoma] 2020 Dec; Vol. 129 (3-4), pp. 275-283. Date of Electronic Publication: 2020 Oct 30.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Highly Rearranged Karyotypes and Multiple Sex Chromosome Systems in Armored Catfishes from the Genus Harttia (Teleostei, Siluriformes).
Autorzy :
Deon GA; Laboratório de Citogenética de Peixes, Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos SP 13565-905, Brazil.; Laboratório de Biologia Cromossômica, Estrutura e Função, Departamento de Biologia Estrutural, Molecular e Genética, Universidade Estadual de Ponta Grossa, Ponta Grossa PR 84030-900, Brazil.
Glugoski L; Laboratório de Citogenética de Peixes, Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos SP 13565-905, Brazil.; Laboratório de Biologia Cromossômica, Estrutura e Função, Departamento de Biologia Estrutural, Molecular e Genética, Universidade Estadual de Ponta Grossa, Ponta Grossa PR 84030-900, Brazil.
Vicari MR; Laboratório de Biologia Cromossômica, Estrutura e Função, Departamento de Biologia Estrutural, Molecular e Genética, Universidade Estadual de Ponta Grossa, Ponta Grossa PR 84030-900, Brazil.
Nogaroto V; Laboratório de Biologia Cromossômica, Estrutura e Função, Departamento de Biologia Estrutural, Molecular e Genética, Universidade Estadual de Ponta Grossa, Ponta Grossa PR 84030-900, Brazil.
Sassi FMC; Laboratório de Citogenética de Peixes, Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos SP 13565-905, Brazil.
Cioffi MB; Laboratório de Citogenética de Peixes, Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos SP 13565-905, Brazil.
Liehr T; Institute of Human Genetics, University Hospital Jena, 07747 Jena, Germany.
Bertollo LAC; Laboratório de Citogenética de Peixes, Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos SP 13565-905, Brazil.
Moreira-Filho O; Laboratório de Citogenética de Peixes, Departamento de Genética e Evolução, Universidade Federal de São Carlos, São Carlos SP 13565-905, Brazil.
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Źródło :
Genes [Genes (Basel)] 2020 Nov 18; Vol. 11 (11). Date of Electronic Publication: 2020 Nov 18.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Novel insights into the mixed germ cell-sex cord stromal tumor of the testis: detection of chromosomal aneuploidy and further morphological evidence supporting the neoplastic nature of the germ cell component.
Autorzy :
Michalova K; Department of Pathology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic. .
McKenney JK; Department of Pathology, Cleveland Clinic, Robert J. Tomsich Pathology & Laboratory Medicine Institute, Cleveland, OH, USA.
Kristiansen G; Department of Pathology, Universitätsklinikum Bonn, 53127, Bonn, Germany.
Steiner P; Bioptical laboratory, Ltd., 301 00, Pilsen, Czech Republic.
Grossmann P; Bioptical laboratory, Ltd., 301 00, Pilsen, Czech Republic.
Putzova M; Bioptical laboratory, Ltd., 301 00, Pilsen, Czech Republic.
Martinek P; Bioptical laboratory, Ltd., 301 00, Pilsen, Czech Republic.
Chottova-Dvorakova M; Department of Physiology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Michal M; Department of Pathology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.; Biomedical Center, Faculty of Medicine in Pilsen, Charles University, 323 00, Pilsen, Czech Republic.
Hes O; Department of Pathology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
Michal M; Department of Pathology, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
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Źródło :
Virchows Archiv : an international journal of pathology [Virchows Arch] 2020 Nov; Vol. 477 (5), pp. 615-623. Date of Electronic Publication: 2020 May 23.
Typ publikacji :
Journal Article
MeSH Terms :
Aneuploidy*
Chromosomes, Human*
Biomarkers, Tumor/*genetics
Neoplasms, Germ Cell and Embryonal/*genetics
Neoplasms, Germ Cell and Embryonal/*pathology
Sex Cord-Gonadal Stromal Tumors/*genetics
Sex Cord-Gonadal Stromal Tumors/*pathology
Testicular Neoplasms/*genetics
Testicular Neoplasms/*pathology
Adult ; Aged ; Biomarkers, Tumor/analysis ; Biopsy ; Comparative Genomic Hybridization ; Genetic Predisposition to Disease ; High-Throughput Nucleotide Sequencing ; Humans ; Immunohistochemistry ; Male ; Middle Aged ; Neoplasms, Germ Cell and Embryonal/chemistry ; Phenotype ; Sex Cord-Gonadal Stromal Tumors/chemistry ; Testicular Neoplasms/chemistry
Czasopismo naukowe
Tytuł :
[The role of new molecular tests in the diagnosis of melanoma in a setting of congenital nævus in an infant].
Autorzy :
Masson Regnault M; Service de dermatologie, centre de références de maladies rares de la peau et des muqueuses, université Paul-Sabatier, hôpital Larrey, CHU de Toulouse, 24, chemin du Pouvourville, 31400 Toulouse, France; Pathology department, Samaritan Drive, San Jose, États-Unis. Electronic address: .
Fraitag S; Service d'anatomopathologie, groupe hospitalier Necker-Enfants-Malades, AP-HP, Paris, France.
Lamant L; Service d'anatomopathologie, CHU de Toulouse, Toulouse, France.
Maza A; Service de dermatologie, centre de références de maladies rares de la peau et des muqueuses, université Paul-Sabatier, hôpital Larrey, CHU de Toulouse, 24, chemin du Pouvourville, 31400 Toulouse, France.
De la Fouchardière A; Service d'anatomopathologie, CHU de Lyon, Lyon, France.
Tournier E; Service d'anatomopathologie, CHU de Lyon, Lyon, France.
Lauwers F; Service de chirurgie maxillo-faciale, CHU Purpan, Toulouse, France.
Carfagna L; Service d'oncodermatologie, institut universitaire du Cancer, Toulouse-Oncopole, CHU de Toulouse, Toulouse, France.
Meyer N; Service d'oncodermatologie, institut universitaire du Cancer, Toulouse-Oncopole, CHU de Toulouse, Toulouse, France.
De Berail A; Service de chirurgie maxillo-faciale, CHU Purpan, Toulouse, France.
Busam KJ; Pathology department, Memorial Sloan-Kettering Cancer Center, New York, États-Unis.
Lazova R; Pathology department, Samaritan Drive, San Jose, États-Unis; Service de dermatologie, hôpital Jean-Bernard, CHU de Poitiers, Poitiers, France.
Mazereeuw-Hautier J; Service de dermatologie, centre de références de maladies rares de la peau et des muqueuses, université Paul-Sabatier, hôpital Larrey, CHU de Toulouse, 24, chemin du Pouvourville, 31400 Toulouse, France.
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Transliterated Title :
Apport des nouveaux tests moléculaires dans le diagnostic d’un mélanome sur nævus congénital chez un nourrisson.
Źródło :
Annales de dermatologie et de venereologie [Ann Dermatol Venereol] 2020 Nov; Vol. 147 (11), pp. 746-754. Date of Electronic Publication: 2020 May 22.
Typ publikacji :
Case Reports; English Abstract
Raport
Tytuł :
Myelodysplastic syndromes in a pediatric patient with Cri du Chat syndrome with a ring chromosome 5.
Autorzy :
Nozawa A; Department of Pediatrics, Graduate School of Medicine, Gifu University, 1-1 Yanagido, Gifu, 501-1194, Japan.
Ozeki M; Department of Pediatrics, Graduate School of Medicine, Gifu University, 1-1 Yanagido, Gifu, 501-1194, Japan. .
Yasue S; Department of Pediatrics, Graduate School of Medicine, Gifu University, 1-1 Yanagido, Gifu, 501-1194, Japan.
Endo S; Department of Pediatrics, Graduate School of Medicine, Gifu University, 1-1 Yanagido, Gifu, 501-1194, Japan.
Kadowaki T; Department of Pediatrics, National Hospital Organization Nagara Medical Center, Gifu, 502-8558, Japan.
Ohnishi H; Department of Pediatrics, Graduate School of Medicine, Gifu University, 1-1 Yanagido, Gifu, 501-1194, Japan.
Muramatsu H; Department of Pediatrics, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, 466-8650, Japan.
Hama A; Department of Hematology and Oncology, Children's Medical Center, Japanese Red Cross Nagoya First Hospital, Nakamura-ku, Nagoya, 453-8511, Japan.
Takahashi Y; Department of Pediatrics, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, 466-8650, Japan.
Kojima S; Department of Pediatrics, Nagoya University Graduate School of Medicine, Showa-ku, Nagoya, 466-8650, Japan.
Fukao T; Department of Pediatrics, Graduate School of Medicine, Gifu University, 1-1 Yanagido, Gifu, 501-1194, Japan.
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Źródło :
International journal of hematology [Int J Hematol] 2020 Nov; Vol. 112 (5), pp. 728-733. Date of Electronic Publication: 2020 Jun 09.
Typ publikacji :
Journal Article
Czasopismo naukowe
Tytuł :
Follow-up of two adult brothers with homozygous CEP57 pathogenic variants expands the phenotype of Mosaic Variegated Aneuploidy Syndrome.
Autorzy :
Dery T; Service de Génétique, Hospices Civils de Lyon, Bron, France.
Chatron N; Service de Génétique, Hospices Civils de Lyon, Bron, France; Equipe GENDEV, CRNL, INSERM U1028 CNRS UMR5292 Université Claude Bernard Lyon 1, Lyon, France.
Alqahtani A; Service de Génétique, Hospices Civils de Lyon, Bron, France.
Pugeat M; Service d'Endocrinologie, Hospices Civils de Lyon, Bron, France.
Till M; Service de Génétique, Hospices Civils de Lyon, Bron, France.
Edery P; Service de Génétique, Hospices Civils de Lyon, Bron, France; Equipe GENDEV, CRNL, INSERM U1028 CNRS UMR5292 Université Claude Bernard Lyon 1, Lyon, France.
Sanlaville D; Service de Génétique, Hospices Civils de Lyon, Bron, France; Equipe GENDEV, CRNL, INSERM U1028 CNRS UMR5292 Université Claude Bernard Lyon 1, Lyon, France; Institut NeuroMyoGène, CNRS UMR 5310 - INSERM U1217, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, France.
Schluth-Bolard C; Service de Génétique, Hospices Civils de Lyon, Bron, France; Equipe GENDEV, CRNL, INSERM U1028 CNRS UMR5292 Université Claude Bernard Lyon 1, Lyon, France; Institut NeuroMyoGène, CNRS UMR 5310 - INSERM U1217, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, France.
Nicolino M; Service d'Endocrinologie Pédiatrique, Hospices Civils de Lyon, Bron, France.
Lesca G; Service de Génétique, Hospices Civils de Lyon, Bron, France; Equipe GENDEV, CRNL, INSERM U1028 CNRS UMR5292 Université Claude Bernard Lyon 1, Lyon, France; Institut NeuroMyoGène, CNRS UMR 5310 - INSERM U1217, Université de Lyon, Université Claude Bernard Lyon 1, Lyon, France.
Putoux A; Service de Génétique, Hospices Civils de Lyon, Bron, France; Equipe GENDEV, CRNL, INSERM U1028 CNRS UMR5292 Université Claude Bernard Lyon 1, Lyon, France. Electronic address: .
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Źródło :
European journal of medical genetics [Eur J Med Genet] 2020 Nov; Vol. 63 (11), pp. 104044. Date of Electronic Publication: 2020 Aug 28.
Typ publikacji :
Journal Article; Review
Czasopismo naukowe
Tytuł :
Genomic testing and counseling: The contribution of next‐generation sequencing to epilepsy genetics.
Autorzy :
Alsubaie, Lamia (AUTHOR)
Aloraini, Taghrid (AUTHOR)
Amoudi, Manal (AUTHOR)
Swaid, Abdulrahman (AUTHOR)
Eyiad, Wafaa (AUTHOR)
Al Mutairi, Fuad (AUTHOR)
Ababneh, Farouq (AUTHOR)
Alrifai, Muhammad Talal (AUTHOR)
Baarmah, Duaa (AUTHOR)
Altwaijri, Waleed (AUTHOR)
Alotaibi, Naser (AUTHOR)
Harthi, Ashraf (AUTHOR)
Rumayyan, Ahmad (AUTHOR)
Alanazi, Ali (AUTHOR)
Qrimli, Mohammad (AUTHOR)
Alfadhel, Majid (AUTHOR)
Alfares, Ahmed (AUTHOR)
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Źródło :
Annals of Human Genetics. Nov2020, Vol. 84 Issue 6, p431-436. 6p.
Czasopismo naukowe
Tytuł :
Bifid nose as the sole manifestation of BNAR syndrome, a FREM1‐related condition.
Autorzy :
Brischoux‐Boucher, Elise
Dahlen, Eric
Gronier, Céline
Nobili, François
Marcoux, Estelle
Alkuraya, Fowzan S.
Van Maldergem, Lionel
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Temat :
NOSE
CHONDROITIN sulfate proteoglycan
SYNDROMES
EXTRACELLULAR matrix proteins
COMPARATIVE genomic hybridization
DENTAL enamel
Źródło :
Clinical Genetics; Nov2020, Vol. 98 Issue 5, p515-516, 2p
Czasopismo naukowe
Tytuł :
Highly Rearranged Karyotypes and Multiple Sex Chromosome Systems in Armored Catfishes from the Genus Harttia (Teleostei, Siluriformes)
Autorzy :
Geize Aparecida Deon
Larissa Glugoski
Marcelo Ricardo Vicari
Viviane Nogaroto
Francisco de Menezes Cavalcante Sassi
Marcelo de Bello Cioffi
Thomas Liehr
Luiz Antonio Carlos Bertollo
Orlando Moreira-Filho
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Temat :
chromosomal rearrangements
comparative genomic hybridization
fish mapping
fish species
karyotype evolution
sex chromosomes
Genetics
QH426-470
Źródło :
Genes, Vol 11, Iss 1366, p 1366 (2020)
Opis pliku :
electronic resource
Relacje :
https://www.mdpi.com/2073-4425/11/11/1366; https://doaj.org/toc/2073-4425
Dostęp URL :
https://doaj.org/article/3b71a1dcf33b406a9882ca8c2f55cbc9
Czasopismo naukowe
Tytuł :
Identification of a cryptic submicroscopic deletion using a combination of fluorescence in situ hybridization and array comparative genomic hybridization in a t(3;5)(q25;q35)-positive acute myeloid leukemia patient: A case report and review of the literature.
Autorzy :
Gao M; Department of Pediatrics, the First Hospital of Jilin University, Changchun City, Jilin.
Li S; Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
Wang L; Department of Pediatrics, the First Hospital of Jilin University, Changchun City, Jilin.
Nie S; Department of Pediatrics, the First Hospital of Jilin University, Changchun City, Jilin.
Pang H; Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
Lu X; Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
Wang X; Department of Pediatrics, University of Oklahoma Health Sciences Center, Oklahoma City, Oklahoma.
Wang M; Department of Radiotherapy, Public Health School of Jilin University, Changchun City, Jilin, P.R. China.
Guo S; Department of Pediatrics, the First Hospital of Jilin University, Changchun City, Jilin.
Ma Y; Department of Pediatrics, the First Hospital of Jilin University, Changchun City, Jilin.
Meng F; Department of Pediatrics, the First Hospital of Jilin University, Changchun City, Jilin.
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Źródło :
Medicine [Medicine (Baltimore)] 2020 Oct 23; Vol. 99 (43), pp. e22789.
Typ publikacji :
Case Reports; Journal Article
MeSH Terms :
Leukemia, Myeloid, Acute/*genetics
Antineoplastic Combined Chemotherapy Protocols/therapeutic use ; Chromosome Banding ; Comparative Genomic Hybridization ; Humans ; In Situ Hybridization, Fluorescence ; Leukemia, Myeloid, Acute/drug therapy ; Male ; Middle Aged
Czasopismo naukowe
Tytuł :
Utility of Hypotonia Diagnostic Investigations: A 12-year Single Center Study.
Autorzy :
AlBanji MH; Department of Neuroscience, King Fahad Medical City, Riyadh, Saudi Arabia.
AlSaad AN; Department of neuroradiology, King Fahad Medical City, Riyadh, Saudi Arabia.
AlAnazi RF; Department of Neuroscience, King Fahad Medical City, Riyadh, Saudi Arabia.
Aleisa ZA; Department of Neuroscience, King Fahad Medical City, Riyadh, Saudi Arabia.
Alam DS; Department of Neuroscience, King Fahad Medical City, Riyadh, Saudi Arabia.
Alhashim AH; Department of Neuroscience, King Fahad Medical City, Riyadh, Saudi Arabia.
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Źródło :
Molecular genetics and metabolism reports [Mol Genet Metab Rep] 2020 Oct 21; Vol. 25, pp. 100665. Date of Electronic Publication: 2020 Oct 21 (Print Publication: 2020).
Typ publikacji :
Journal Article
Czasopismo naukowe

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