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American Journal of Human Genetics|December 1, 2009
Deletions and point mutations of LRRC50 cause primary ciliary dyskinesia due to dynein arm defectsNiki Tomas Loges, Heike Olbrich, Anita Becker-Heck, et al.American Journal of Human Genetics|March 1, 1979
The biochemical genetics of the hexosaminidase system in manE BeutlerAmerican Journal of Human Genetics|January 1, 1985
Mother-child HLA compatibility ratios in children of Amerinidian parents who share common haplotypesF L BlackAmerican Journal of Human Genetics|January 1, 1985
Family-size distribution and Ewens' equivalence theoremS E HodgeAmerican Journal of Human Genetics|September 1, 1987
Characterization of human centromeric regions of specific chromosomes by means of alphoid DNA sequencesE W Jabs, M G PersicoAmerican Journal of Human Genetics|September 1, 1987
Structural analysis of normal and mutant insulin receptors in fibroblasts cultured from families with leprechaunismF Endo, N Nagata, J H Priest, et al.American Journal of Human Genetics|September 1, 1986
Contrasting evolutionary histories among tightly linked HLA lociW Klitz, G Thomson, M P BaurAmerican Journal of Human Genetics|September 1, 1986
Family study on the polymorphisms of the sixth and seventh components (C6 and C7) of human complement: linkage and haplotype analysesK Tokunaga, G Dewald, K Omoto, et al.American Journal of Human Genetics|May 1, 1985
Segregation and fertility analysis in an autosomal reciprocal translocation, t(1;8)(q41;q23.1)A E Vauhkonen, E M Sankila, K O Simola, et al.American Journal of Human Genetics|November 1, 1986
The incidence and gene frequency of ataxia-telangiectasia in the United StatesM Swift, D Morrell, E Cromartie, et al.Pageof 980