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Journal 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.Journal of Human Genetics|March 20, 2010
Family-based association study of IGF1 microsatellites and height, weight, and body mass indexGordon Fehringer, Hilmi Ozcelik, Julia A Knight, et al.Journal of Human Genetics|December 17, 2003
Combined effects of PPARgamma2 P12A and PPARalpha L162V polymorphisms on glucose and insulin homeostasis: the Québec Family StudyYohan Bossé, S John Weisnagel, Claude Bouchard, et al.Journal of Human Genetics|May 1, 2004
Up-regulation of transcriptional factor E2F1 in papillary and anaplastic thyroid cancersMasamitsu Onda, Hisaki Nagai, Akira Yoshida, et al.Journal of Human Genetics|August 13, 2005
Etiopathogenesis of arrhythmogenic right ventricular cardiomyopathyMaithili V N Dokuparti, Pranathi Rao Pamuru, Bhavesh Thakkar, et al.Pageof 351