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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.Journal of Human Genetics|October 24, 2000
Multiplex PCR amplification of TH01, D9S304, and D3S1744 lociK Fujii, H Senju, K Yoshida, et al.Journal of Human Genetics|October 24, 2000
cDNA cloning of a human RAB26-related gene encoding a Ras-like GTP-binding protein on chromosome 16p13.3 regionN Seki, T Yoshikawa, A Hattori, et al.Journal of Human Genetics|April 3, 2001
Amino-acid substitutions in the IKAP gene product significantly increase risk for bronchial asthma in childrenS Takeoka, M Unoki, Y Onouchi, et al.Journal of Human Genetics|November 22, 2017
Application of genome editing technologies in rats for human disease modelsKazuto Yoshimi, Tomoji MashimoPageof 353