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Journal of Human Genetics|December 16, 1998
Cloning, expression analysis, and chromosomal localization of HIP1R, an isolog of huntingtin interacting protein (HIP1)N Seki, M Muramatsu, S Sugano, et al.Journal of Human Genetics|December 16, 1998
A HhaI/BstUI polymorphism in a novel gene at human chromosome 11p15.5K Miura, H Masuzaki, T Ishimaru, et al.Journal of Human Genetics|December 16, 1998
Isolation of a polymorphic CA repeat sequence at the human progesterone receptor (PGR) locusK Tsukamoto, I Watanabe, T Shiba, et al.Journal of Human Genetics|February 3, 2006
Molecular insights into the origins of the Shompen, a declining population of the Nicobar archipelagoRajni Trivedi, T Sitalaximi, Jheelam Banerjee, et al.Journal of Human Genetics|February 3, 2006
Biochemical data in ornithine transcarbamylase deficiency (OTCD) carrier risk estimation: logistic discrimination and combination with genetic informationKonrad OexleJournal of Human Genetics|February 8, 2006
A rapid and reliable detection system for the analysis of PMP22 gene dosage by MP/DHPLC assayChia-Yun Lin, Yi-Ning Su, Chien-Nan Lee, et al.Journal of Human Genetics|January 19, 2006
De novo COX2 mutation in a LHON family of Caucasian origin: implication for the role of mtDNA polymorphism in human pathologySergey I Zhadanov, Vasiliy V Atamanov, Nikolay I Zhadanov, et al.Journal of Human Genetics|January 24, 2006
Association of IL8, CXCR2 and TNF-alpha polymorphisms and airway diseaseMelanie C Matheson, Justine A Ellis, Joan Raven, et al.Journal of Human Genetics|May 20, 2008
Association of genetic variations of genes encoding thrombospondin, type 1, domain-containing 4 and 7A with low bone mineral density in Japanese women with osteoporosisSeijiro Mori, Ikuyo Kou, Hidenori Sato, et al.Journal of Human Genetics|April 11, 2008
Positive association of the FTSJ1 gene polymorphisms with nonsyndromic X-linked mental retardation in young Chinese male subjectsLing Dai, Lianxi Xing, Pingyuan Gong, et al.Pageof 353