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Human Heredity|January 1, 1979
Seven cases of branchial cyst and sinuses in four generationsT S Anand, C S Anand, B D ChaurasiaHuman Heredity|January 1, 1979
Genetic and nongenetic influences on the ABH and Lea antigen levels of saliva and milkR Barrantes, F M SalzanoHuman Heredity|September 28, 1998
160Thr mutation in the rhodopsin gene associated with retinitis pigmentosaC Capeans, M J Blanco, M V Lareu, et al.Human Heredity|September 28, 1998
New DNA polymorphisms define ethnically distinct haplotypes in the human transferrin receptor geneG F Van Landeghem, L E Beckman, C Sikström, et al.Human Heredity|September 28, 1998
DNA analysis of the fragile X syndrome in an at risk pediatric population in croatia: simple clinical preselection criteria can considerably improve the cost-effectiveness of fragile X screening studiesS Hećimović, I Barisić, K PavelićHuman Heredity|September 28, 1998
No evidence for an association between a variant of the mast cell chymase gene and atopic dermatitis based on case-control and haplotype-relative-risk analysesT Kawashima, E Noguchi, T Arinami, et al.Human Heredity|January 1, 1979
Association between Duffy blood groups and serum level of the pregnancy zone proteinL Beckman, K Bergdahl, B Cedergren, et al.Human Heredity|January 1, 1979
Segregation and linkage analyses of dopamine-beta-hydroxylase activityR C Elston, K K Namboodiri, C G HamesPageof 237