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Journal of Human Genetics|September 6, 2005
Isolates in a corridor of migrations: a high-resolution analysis of Y-chromosome variation in JordanCarlos Flores, Nicole Maca-Meyer, Jose M Larruga, et al.Journal of Human Genetics|May 4, 2006
CSNB1 in Chinese families associated with novel mutations in NYXXueshan Xiao, Xiaoyun Jia, Xiangming Guo, et al.Journal of Human Genetics|April 15, 2006
A -16C>T substitution in the 5' UTR of the puratrophin-1 gene is prevalent in autosomal dominant cerebellar ataxia in NaganoTakako Ohata, Kunihiro Yoshida, Haruya Sakai, et al.Journal of Human Genetics|April 28, 2006
Humanin expression in skeletal muscles of patients with chronic progressive external ophthalmoplegiaTesseki Kin, Kazuma Sugie, Makito Hirano, et al.Journal of Human Genetics|May 2, 2006
Analyses of 5' regulatory region polymorphisms in human SLC22A6 (OAT1) and SLC22A8 (OAT3)Vibha Bhatnagar, Gang Xu, Bruce A Hamilton, et al.Journal of Human Genetics|March 18, 2006
Complete hydatidiform mole and normal live birth following intracytoplasmic sperm injectionHaruka Hamanoue, Nobuko Umezu, Mika Okuda, et al.Journal of Human Genetics|March 18, 2006
Is there any evidence for linkage on chromosome 17cen in affected Japanese sib-pairs with an intracranial aneurysm?Boris Krischek, Akira Narita, Hiroyuki Akagawa, et al.Journal of Human Genetics|February 27, 2004
Association of the T-cell regulatory gene CTLA4 with Graves' disease and autoimmune thyroid disease in the JapaneseKoichi Furugaki, Senji Shirasawa, Naofumi Ishikawa, et al.Journal of Human Genetics|March 3, 2004
Rapid isolation of viral integration site reveals frequent integration of HTLV-1 into expressed lociTatsuhiko Ozawa, Takahiro Itoyama, Naoki Sadamori, et al.Pageof 351