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Journal of Human Genetics|July 29, 2011
Identification of two HEXA mutations causing infantile-onset Tay-Sachs disease in the Persian populationAlireza Haghighi, Jamileh Rezazadeh, Azam Ahmadi Shadmehri, et al.Journal of Human Genetics|July 29, 2011
Genetic association analysis of TAP1 and TAP2 polymorphisms with aspirin exacerbated respiratory disease and its FEV1 declineJeong-Hyun Kim, Byung-Lae Park, Charisse Flerida A Pasaje, et al.Journal of Human Genetics|November 4, 2011
Genome-wide association study of copy number variation identified gremlin1 as a candidate gene for lean body massRong Hai, Yu-Fang Pei, Hui Shen, et al.Journal of Human Genetics|November 4, 2011
A family-based association study of DIO2 and children mental retardation in the Qinba region of ChinaKejin Zhang, Heng Xi, Xiying Wang, et al.Journal of Human Genetics|August 12, 2011
Integration-free and stable expression of FVIII using a human artificial chromosomeHajime Kurosaki, Masaharu Hiratsuka, Natsuko Imaoka, et al.Journal of Human Genetics|August 26, 2011
Tandem configurations of variably duplicated segments of 22q11.2 confirmed by fiber-FISH analysisKeiko Shimojima, Nobuhiko Okamoto, Tetsuya Inazu, et al.Journal of Human Genetics|September 23, 2011
Support for association between the Ser205Leu polymorphism of p75(NTR) and major depressive disorderTakashi Fujii, Noriko Yamamoto, Hiroaki Hori, et al.Journal of Human Genetics|October 28, 2011
Uneventful clinical courses of Korean patients with methylcrotonylglycinuria and their common mutationsChang-Woo Jung, Beom Hee Lee, Joo Hyun Kim, et al.Journal of Human Genetics|September 16, 2011
HVS-I polymorphism screening of ancient human mitochondrial DNA provides evidence for N9a discontinuity and East Asian haplogroups in the Neolithic HungaryZsuzsanna Guba, Éva Hadadi, Ágnes Major, et al.Journal of Human Genetics|February 4, 2012
SNP rs11190870 near LBX1 is associated with adolescent idiopathic scoliosis in southern ChineseYan-Hui Fan, You-Qiang Song, Danny Chan, et al.Pageof 351