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Journal of Human Genetics|May 12, 2000
Disparity between association and linkage analysis for HNF1A G319S in type 2 diabetes in Canadian Oji-CreeR A Hegele, A J Hanley, B Zinman, et al.Journal of Human Genetics|May 12, 2000
Molecular cloning and expression analysis of the human DA41 gene and its mapping to chromosome 9q21.2-q21.3E Hanaoka, T Ozaki, M Ohira, et al.Journal of Human Genetics|May 13, 1999
Molecular characterization of 6-pyruvoyl-tetrahydropterin synthase deficiency in Japanese patientsT Imamura, Y Okano, H Shintaku, et al.Journal of Human Genetics|May 13, 1999
Germline mutations of E-cadherin gene in Korean familial gastric cancer patientsK A Yoon, J L Ku, H K Yang, et al.Journal of Human Genetics|May 13, 1999
The fusion gene at the ABO-secretor locus (FUT2): absence in Chinese populationsY H Liu, Y Koda, M Soejima, et al.Journal of Human Genetics|March 20, 1999
Molecular epidemiology of C9 deficiency heterozygotes with an Arg95Stop mutation of the C9 gene in JapanR Kira, K Ihara, K Watanabe, et al.Journal of Human Genetics|March 20, 1999
Isolation and characterization of a novel serine threonine kinase gene on chromosome 3p22-21.3M Tamari, Y Daigo, Y NakamuraJournal of Human Genetics|March 20, 1999
A novel human gene whose product shares significant homology with the bovine brain-specific protein p25 on chromosome 5p15.3N Seki, A Hattori, S Sugano, et al.Journal of Human Genetics|October 24, 2000
Molecular analysis of Wilson disease in Taiwan: identification of one novel mutation and evidence of haplotype-mutation associationC C Lee, J Y Wu, F J Tsai, et al.Journal of Human Genetics|October 24, 2000
Association of the vitamin D receptor start codon polymorphism (FokI) with bone mineral density in postmenopausal Korean womenY M Choi, J K Jun, J Choe, et al.Pageof 352