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Human Heredity|January 1, 1975
Amylo-1,60glucosidase deficiency (glycogenosis type III) in the Faroe IslandsJ Cohn, P Wang, M Hauge, et al.Human Heredity|June 12, 1999
Localization of the gene responsible for familial benign polycythemia to chromosome 11q23N N Vasserman, L M Karzakova, S M Tverskaya, et al.Human Heredity|June 12, 1999
New AccI polymorphism in the follicle-stimulating hormone beta-subunit gene and its prevalence in three Southeast Asian populationsW X Liao, Y Tong, A C Roy, et al.Human Heredity|August 7, 1999
Identification of a new transthyretin variant (Ile49) in familial amyloidotic polyneuropathy using electrospray ionization mass spectrometry and nonisotopic RNase cleavage assayM Nakamura, T Yamashita, Y Ando, et al.Human Heredity|August 7, 1999
Ethnic variation in the mitochondrial targeting sequence polymorphism of MnSODG F Van Landeghem, P Tabatabaie, V Kucinskas, et al.Human Heredity|August 7, 1999
Multipoint linkage analysis. A cautionary noteJ Halpern, A S WhittemoreHuman Heredity|November 5, 1999
Progressing from eugenics to human genetics. celebrating the 70th birthday of professor Newton E. MortonC C LiHuman Heredity|November 5, 1999
The future of path analysis, segregation analysis, and combined models for genetic dissection of complex traitsD C Rao, M A ProvinceHuman Heredity|November 5, 1999
Haplotyping in pedigrees via a genetic algorithmP Tapadar, S Ghosh, P P MajumderPageof 237