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Journal of Human Genetics|October 27, 2006
A novel de novo frame-shift mutation of the EDA gene in a Chinese Han family with hypohidrotic ectodermal dysplasiaChangzheng Huang, Qinbo Yang, Tie Ke, et al.Journal of Human Genetics|October 7, 2006
Genetic structural differences between responders and non-responders to interferon therapy for chronic hepatitis-B patientsPei-Jer Chen, Cherry Guan-Ju Lin, Felicia Yi-Fang Lin, et al.Journal of Human Genetics|October 7, 2006
Identification of chromosomal regions linked to premature myocardial infarction: a meta-analysis of whole-genome searchesElias Zintzaras, Georgios KitsiosJournal of Human Genetics|October 13, 2006
DNA-based diagnosis of malignant osteopetrosis by whole-genome scan using a single-nucleotide polymorphism microarray: standardization of molecular investigations of genetic diseases due to consanguinityChing-Wan Lam, Sui-Fan Tong, Keong Wong, et al.Journal of Human Genetics|October 13, 2006
Ankyrin G overexpression in Hutchinson-Gilford progeria syndrome fibroblasts identified through biological filtering of expression profilesJian Wang, John F Robinson, Caroline H O'Neil, et al.Journal of Human Genetics|July 15, 2004
Common founder effect of rapsyn N88K studied using intragenic markersVanessa Dunne, Ricardo A MaselliJournal of Human Genetics|July 15, 2004
Trisomy 1 in a case of a missed abortionMichio Banzai, Satoshi Sato, Hideo Matsuda, et al.Journal of Human Genetics|September 7, 2004
Glucose-6-phosphate dehydrogenase (G6PD) mutations in Myanmar: G6PD Mahidol (487G>A) is the most common variant in the Myanmar populationHiroyuki Matsuoka, Jichun Wang, Makoto Hirai, et al.Journal of Human Genetics|September 15, 2004
Characterization of the human nasal embryonic LHRH factor gene, NELF, and a mutation screening among 65 patients with idiopathic hypogonadotropic hypogonadism (IHH)Kiyonori Miura, James S Acierno, Stephanie B SeminaraJournal of Human Genetics|September 15, 2004
Polymorphisms within a polymorphism: SNPs in and around a polymorphic Alu insertion in intron 44 of the human dystrophin geneAlan D Lovell, Vania Yotova, Fengxia Xiao, et al.Pageof 353