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Journal of Human Genetics|November 18, 2006
Human organic cation transporter (OCT1 and OCT2) gene polymorphisms and therapeutic effects of metforminEriko Shikata, Rei Yamamoto, Hiroshi Takane, et al.Journal of Human Genetics|July 18, 2006
Mutational screening of ARX gene in Brazilian males with mental retardation of unknown etiologyRaquel de Souza Gestinari-Duarte, Cíntia Barros Santos-Rebouças, Márcia Mattos Gonçalves PimentelJournal of Human Genetics|December 13, 2006
A genomewide linkage analysis of Kawasaki disease: evidence for linkage to chromosome 12Yoshihiro Onouchi, Mayumi Tamari, Atsushi Takahashi, et al.Journal of Human Genetics|December 21, 2006
Glucocorticoid-induced alternative promoter usage for a novel 5' variant of granzyme AYoshinao Ruike, Susumu Katsuma, Akira Hirasawa, et al.Journal of Human Genetics|December 21, 2006
Genetic polymorphisms associated with adverse events and elimination of methotrexate in childhood acute lymphoblastic leukemia and malignant lymphomaHiroyuki Imanishi, Noboru Okamura, Mariko Yagi, et al.Journal of Human Genetics|December 21, 2006
Haplotype analysis at the alcohol dehydrogenase gene region in New Zealand MāoriDavid A Hall, Geoffrey K Chambers, Rodney A LeaJournal of Human Genetics|December 23, 2006
Hereditary prosopagnosia (HPA): the first report outside the Caucasian populationIngo Kennerknecht, Nina Plümpe, Steve Edwards, et al.Journal of Human Genetics|December 2, 2008
Carrier frequency of GJB2 (connexin-26) mutations causing inherited deafness in the Korean populationSung-Hee Han, Hong-Joon Park, Eun-Joo Kang, et al.Journal of Human Genetics|June 27, 2009
Allele frequencies of the ABCC11 gene for earwax phenotypes among ancient populations of Hokkaido, JapanTakehiro Sato, Tetsuya Amano, Hiroko Ono, et al.Journal of Human Genetics|April 18, 2009
Mutation analysis of COX18 in 29 patients with isolated cytochrome c oxidase deficiencySabrina Sacconi, Leonardo Salviati, Eva TrevissonPageof 353