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Journal of Human Genetics|March 14, 2009
Replication studies for the association of PSMA6 polymorphism with coronary artery disease in East Asian populationsKunihiko Hinohara, Toshiaki Nakajima, Taishi Sasaoka, et al.Journal of Human Genetics|May 23, 2009
A novel single-base deletion in ROR2 causes atypical brachydactyly type B1 with cutaneous syndactyly in a large Chinese familyDan Lv, Yang Luo, Wei Yang, et al.Journal of Human Genetics|May 23, 2009
No association between the brain-derived neurotrophic factor gene and panic disorder in Japanese populationTakeshi Otowa, Takafumi Shimada, Yoshiya Kawamura, et al.Journal of Human Genetics|May 16, 2009
A limited spectrum of phenylalanine hydroxylase mutations is observed in phenylketonuria patients in western Poland and implications for treatment with 6R tetrahydrobiopterinSteven F Dobrowolski, K Borski, C C Ellingson, et al.Journal of Human Genetics|May 16, 2009
Frequencies of genotypes and alleles of the functional SNPs in CYP2C19 and CYP2E1 in mainland Chinese Kazakh, Uygur and Han populationsShu-Mei Wang, An-Ping Zhu, Dan Li, et al.Journal of Human Genetics|February 28, 2009
Construction of a prediction model for type 2 diabetes mellitus in the Japanese population based on 11 genes with strong evidence of the associationKazuaki Miyake, Woosung Yang, Kazuo Hara, et al.Journal of Human Genetics|January 23, 2009
Case-control association study of 59 candidate genes reveals the DRD2 SNP rs6277 (C957T) as the only susceptibility factor for schizophrenia in the Bulgarian populationElitza T Betcheva, Taisei Mushiroda, Atsushi Takahashi, et al.Journal of Human Genetics|January 23, 2009
Origins of the Moken Sea Gypsies inferred from mitochondrial hypervariable region and whole genome sequencesKelsey Needham Dancause, Chim W Chan, Narumon Hinshiranan Arunotai, et al.Journal of Human Genetics|January 23, 2009
Susceptibility genes for Kawasaki disease: toward implementation of personalized medicineAkira Hata, Yoshihiro OnouchiJournal of Human Genetics|January 23, 2009
Characterization of deletion breakpoints in patients with dystrophinopathy carrying a deletion of exons 45-55 of the Duchenne muscular dystrophy (DMD) geneDaigo Miyazaki, Kunihiro Yoshida, Kazuhiro Fukushima, et al.Pageof 353