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Journal of Human Genetics|July 27, 2012
Next-generation sequencing: impact of exome sequencing in characterizing Mendelian disordersBahareh Rabbani, Nejat Mahdieh, Kazuyoshi Hosomichi, et al.Journal of Human Genetics|August 17, 2012
Mitochondrial diversity patterns and the Magdalenian resettlement of Europe: new insights from the edge of the Franco-Cantabrian refugeAntonio F Pardiñas, Agustín Roca, Eva Garcia-Vazquez, et al.Journal of Human Genetics|September 25, 1998
A novel mutation of coproporphyrinogen oxidase (CPO) gene in a Japanese familyS Susa, M Daimon, I Yamamori, et al.Journal of Human Genetics|September 25, 1998
Molecular phylogenetics of the hominoid Y chromosomeR V Samonte, R A Conte, R S VermaJournal of Human Genetics|September 25, 1998
Y-specific DNA polymorphisms of the YAP element and the locus DYS19 in the Korean populationW Kim, D J Shin, S A You, et al.Journal of Human Genetics|September 25, 1998
Connatal Pelizaeus-Merzbacher disease: a missense mutation in exon 4 of the proteolipid protein (PLP) geneM Nagao, J KadowakiJournal of Human Genetics|September 25, 1998
Dinucleotide repeat polymorphism in the first intron of the CSR geneH J Han, Y NakamuraJournal of Human Genetics|September 25, 1998
Novel polymorphisms in the beta ig-h3 geneM Tsujikawa, Y Shimomura, M Okada, et al.Journal of Human Genetics|June 15, 2012
Mutational analysis of PHEX, FGF23, DMP1, SLC34A3 and CLCN5 in patients with hypophosphatemic ricketsSigne S Beck-Nielsen, Kim Brixen, Jeppe Gram, et al.Journal of Human Genetics|March 20, 2010
Functional impact of a single-nucleotide polymorphism in the OPRD1 promoter regionHuiping Zhang, Joel Gelernter, Jeffrey R Gruen, et al.Pageof 353