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Journal of Human Genetics|March 8, 2003
Mutation analysis of the ALD gene in seven Japanese families with X-linked adrenoleukodystrophyTadashi Matsumoto, Akira Tsuru, Nagisa Amamoto, et al.Journal of Human Genetics|August 16, 2003
Identification of 46 novel SNPs in the 130-kb region containing a myocardial infarction susceptibility gene on chromosomal band 6p21Aritoshi Iida, Kouichi Ozaki, Yozo Ohnishi, et al.Journal of Human Genetics|August 9, 2003
A novel locus for parietal foramina maps to chromosome 4q21-q23Gang Chen, Desan Zhang, Guoying Feng, et al.Journal of Human Genetics|April 14, 2017
A missense variant, rs373863828-A (p.Arg457Gln), of CREBRF and body mass index in Oceanic populationsIzumi Naka, Takuro Furusawa, Ryosuke Kimura, et al.Journal of Human Genetics|April 14, 2017
Update of the GJB2/DFNB1 mutation spectrum in Russia: a founder Ingush mutation del(GJB2-D13S175) is the most frequent among other large deletionsElena A Bliznetz, Maria R Lalayants, Tatiana G Markova, et al.Journal of Human Genetics|March 15, 2008
Structural study on mutant alpha-L-iduronidases: insight into mucopolysaccharidosis type IKanako Sugawara, Seiji Saito, Kazuki Ohno, et al.Journal of Human Genetics|January 12, 2008
IGF-I (CA) repeat polymorphisms and risk of cancer: a meta-analysisXin Chen, Jianming Guan, Yuting Song, et al.Journal of Human Genetics|February 27, 2008
Association of the MSX2 gene polymorphisms with ankylosing spondylitis in JapaneseTatsuya Furuichi, Koichi Maeda, Chung-Tei Chou, et al.Journal of Human Genetics|February 27, 2008
Prediction of functional nonsynonymous single nucleotide polymorphisms in human G-protein-coupled receptorsDan Xue, Jingyuan Yin, Mingfeng Tan, et al.Journal of Human Genetics|March 7, 2008
Identification and characterization of cryptic SHOX intragenic deletions in three Japanese patients with Léri-Weill dyschondrosteosisMaki Fukami, Sumito Dateki, Fumiko Kato, et al.Pageof 353