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المؤلفون: Amanda Krause, Thomy J. L. de Ravel, Neil V. Morgan, Christopher G. Mathew, Linda Wainwright, Hans Joenje, Stander Jansen, Martin Digweed, Marc Tischkowitz, Fahmida Essop, Janet Poole, Ilja Demuth, Cathryn M. Lewis
المساهمون: Clinical sciences, Medical Genetics
المصدر: Blood. 105(9)
مصطلحات موضوعية: FANCG Gene, Immunology, Population, Black People, Cell Cycle Proteins, Biology, Biochemistry, Fanconi anemia, FANCG, medicine, Humans, education, Fanconi Anemia Complementation Group G Protein, Africa South of the Sahara, Sequence Deletion, Genetics, Cell Cycle Proteins/genetics, education.field_of_study, Molecular Epidemiology, Base Sequence, Genetic heterogeneity, Incidence, Haplotype, African Continental Ancestry Group/genetics, Nuclear Proteins, Cell Biology, Hematology, medicine.disease, Africa South of the Sahara/epidemiology, Fanconi Anemia Complementation Group Proteins, Founder Effect, Nuclear Proteins/genetics, DNA-Binding Proteins, Fanconi Anemia, Fanconi Anemia/epidemiology, Haplotypes, Mutation (genetic algorithm), DNA-Binding Proteins/genetics, Founder effect
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af423f0d97fc57017404c43153e67643
https://pubmed.ncbi.nlm.nih.gov/15657175