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المؤلفون: Michael A. Morris, Emmanuèle Barras, Stylianos E. Antonarakis, Jean Villard, Bernard Mach, Walter Reith, Peter J. van den Elsen, Arnaud Gos
المصدر: Human Mutation, Vol. 10, No 6 (1997) pp. 430-435
مصطلحات موضوعية: Male, DNA, Complementary, Genes, MHC Class II, DNA Mutational Analysis, DNA-Binding Proteins/ genetics, Transcription Factors/genetics, Regulatory Factor X Transcription Factors, Biology, Heterozygote Detection, Transcription (biology), Gene expression, Genetics, medicine, Humans, Cloning, Molecular, Genes, MHC Class II/ genetics, Transcription factor, Gene, Genetics (clinical), Regulator gene, ddc:616, Genetic Carrier Screening, Genetic Complementation Test, Bare lymphocyte syndrome, Chromosome Mapping, DNA, Complementary/genetics, Promoter, medicine.disease, Molecular biology, DNA-Binding Proteins, Severe Combined Immunodeficiency/ genetics, Chromosomes, Human, Pair 1/genetics, Chromosomes, Human, Pair 1, Severe Combined Immunodeficiency, Female, RFX5, Transcription Factors
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b1ada142486f9c2fd9a8630500e94277
https://doi.org/10.1002/(sici)1098-1004(1997)10:6<430::aid-humu3>3.0.co;2-h