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Human Genetics|January 1, 1984
Prenatal identification of a deleted Y chromosome by cytogenetics and a Y-specific repetitive DNA probeC Disteche, D Luthy, D B Haslam, et al.Human Genetics|January 1, 1981
Mutagen-induced sister chromatid exchange rate in Bloom syndrome remains unaltered in the presence of Bloom corrective factorU Schmidt-Preuss, P Maack, C R Bartram, et al.Human Genetics|January 1, 1981
Diphenoloxidases in X-linked recessive (Duchenne) muscular dystrophyJ J Demos, D G Tuil, P C Katz, et al.Human Genetics|January 1, 1982
Evidence for the deficiency of beta-glucosidase-activating factor in fibroblasts of patients with I-cell diseaseR Varon, W J Kleijer, E J Thompson, et al.Human Genetics|January 1, 1982
Distribution of physiological adult lactase phenotypes, lactose absorber and malabsorber, in GermanyG Flatz, J N Howell, J Doench, et al.Human Genetics|January 1, 1983
Interactions between C-bands of chromosomes 1 and 9 in recurrent reproductive lossJ H Ford, D F Callen, C G Roberts, et al.Human Genetics|June 1, 1996
Interstitial deletion of chromosome 6q: precise definition of the breakpoints by microdissection, DNA amplification, and reverse paintingN Rubtsov, G Senger, H Kuzcera, et al.Human Genetics|June 1, 1996
Allelic association between a Ser-9-Gly polymorphism in the dopamine D3 receptor gene and schizophreniaS Shaikh, D A Collier, P C Sham, et al.Human Genetics|June 1, 1996
EagI and NotI linking clones from human chromosomes 11 and XpM A Pook, R Thakrar, B Pottinger, et al.Human Genetics|June 1, 1996
Distribution and frequency of a polymorphic Alu insertion at the plasminogen activator locus in humansS A Tishkoff, G Ruano, J R Kidd, et al.Pageof 959