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Journal of Human Genetics|March 21, 2009
Acquisition of inverted GSTM exons by an intron of primate GSTM5 geneYong Wang, Frederick C C LeungJournal of Human Genetics|October 7, 2006
Association study of COL9A2 with lumbar disc disease in the Japanese populationShoji Seki, Yoshiharu Kawaguchi, Masaki Mori, et al.Journal of Human Genetics|December 16, 2006
Association of gene polymorphism with genetic susceptibility to stroke in Asian populations: a meta-analysisIndranil Banerjee, Veena Gupta, Subramaniam GaneshJournal of Human Genetics|June 21, 2007
Testing the hypothesis of an ancient Roman soldier origin of the Liqian people in northwest China: a Y-chromosome perspectiveRuixia Zhou, Lizhe An, Xunling Wang, et al.Journal of Human Genetics|March 14, 2007
The ACVR1 617G>A mutation is also recurrent in three Japanese patients with fibrodysplasia ossificans progressivaMasahiro Nakajima, Nobuhiko Haga, Kazuharu Takikawa, et al.Journal of Human Genetics|March 14, 2007
Two novel nonsense mutations in GALNT3 gene are responsible for familial tumoral calcinosisAnna Maria Barbieri, Marcello Filopanti, Guido Bua, et al.Journal of Human Genetics|June 15, 2007
Association of the HTRA1 gene variant with age-related macular degeneration in the Japanese populationKeisuke Mori, Kuniko Horie-Inoue, Masakazu Kohda, et al.Journal of Human Genetics|September 4, 2007
Oculocutaneous albinism type 2 (OCA2) with homozygous 2.7-kb deletion of the P gene and sickle cell disease in a Cameroonian family. Identification of a common TAG haplotype in the mutated P geneRobert Aquaron, Nadem Soufir, Jean-Louis Bergé-Lefranc, et al.Journal of Human Genetics|September 5, 2007
Role of genetic polymorphisms in ACE and TNF-alpha gene in sarcoidosis: a meta-analysisIgor Medica, Andrej Kastrin, Ales Maver, et al.Journal of Human Genetics|August 9, 2008
A novel missense mutation in the EDA gene associated with X-linked recessive isolated hypodontiaMahmood Rasool, Jens Schuster, Muhammad Aslam, et al.Pageof 353