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Annals of Human Genetics|March 29, 2000
Statistical genetic analysis of plasma levels of vitamin D: familial studyG Livshits, D Karasik, M J SeibelAnnals of Human Genetics|March 30, 2000
Mucopolysaccharidosis type I: characterization of a common mutation that causes Hurler syndrome in Moroccan subjectsN Alif, K Hess, J Straczek, et al.Annals of Human Genetics|March 30, 2000
An Asian-Native American paternal lineage identified by RPS4Y resequencing and by microsatellite haplotypingA W Bergen, C Y Wang, J Tsai, et al.Annals of Human Genetics|March 30, 2000
Enzymatic characterization of four new mutations in the glucose-6 phosphatase (G6PC) gene which cause glycogen storage disease type 1aN Bruni, F Rajas, S Montano, et al.Annals of Human Genetics|March 30, 2000
Supportive evidence for contribution of the dopamine D2 receptor gene to heritability of stature: linkage and association studiesT Arinami, Y Iijima, K Yamakawa-Kobayashi, et al.Annals of Human Genetics|March 30, 2000
Assessing linkage disequilibrium in a complex genetic system. I. Overall deviation from random associationH Zhao, A J Pakstis, J R Kidd, et al.Annals of Human Genetics|March 30, 2000
Linkage disequilibrium between intra-locus variants in the aminopeptidase n gene and test of their association with coeliac diseaseM Giordano, E Bolognesi, S D'Alfonso, et al.Annals of Human Genetics|March 30, 2000
Common HLA alleles, rather than rare mutants, confer susceptibility to coeliac diseaseP M Brett, J Y Yiannakou, M A Morris, et al.Annals of Human Genetics|January 31, 2003
Haplotype structure of TP53 locus in Indian population and possible association with head and neck cancerS Mitra, S Chatterjee, C K Panda, et al.Pageof 231