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Journal of Human Genetics|May 24, 2003
Hypertriglyceridemia associated with amino acid variation Asn985Tyr of the RP1 geneYuko Fujita, Yoichi Ezura, Mitsuru Emi, et al.Journal of Human Genetics|May 30, 2003
The role of the IKAP gene polymorphisms in atopic diseases in the middle European populationMarcel Schüller, Lydie Izakovičová Hollá, Dana Bučková, et al.Journal of Human Genetics|May 13, 2003
Association of single-nucleotide polymorphisms in the polymeric immunoglobulin receptor gene with immunoglobulin A nephropathy (IgAN) in Japanese patientsWataru Obara, Aritoshi Iida, Yasushi Suzuki, et al.Journal of Human Genetics|May 28, 2003
Molecular cloning and characterization of a novel human J-domain protein gene (HDJ3) from the fetal brainJuxiang Chen, Yan Huang, Hai Wu, et al.Journal of Human Genetics|May 28, 2003
Association study of autoimmune thyroid disease at 5q23-q33 in Japanese patientsTakashi Akamizu, Hitomi Hiratani, Satoshi Ikegami, et al.Journal of Human Genetics|May 28, 2003
LMNA is mutated in Hutchinson-Gilford progeria (MIM 176670) but not in Wiedemann-Rautenstrauch progeroid syndrome (MIM 264090)Henian Cao, Robert A HegeleJournal of Human Genetics|September 19, 2003
Molecular genetics of autism spectrum disordersBarkur S ShastryJournal of Human Genetics|September 19, 2003
Power of association test for detecting minor histocompatibility gene causing graft-versus-host disease following bone marrow transplantation [correction]Jun Ohashi, Etsuko Maruya, Katsushi Tokunaga, et al.Journal of Human Genetics|May 6, 2003
High-density SNP map of human ITR, a gene associated with vascular remodelingAritoshi Iida, Toshihiro Tanaka, Yusuke NakamuraJournal of Human Genetics|May 6, 2003
A pair of sibs with tibial hemimelia born to phenotypically normal parentsJuntaro Matsuyama, Akihiko Mabuchi, Junwei Zhang, et al.Pageof 353