journal of human genetics سال:2017 - دوره:62

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journal of human genetics
سال:2017 - دوره:62 - شماره:3

A combined linkage and association strategy identifies a variant near the GSTP1 gene associated with BMI in the Mexican population - صفحه:413-418 Association of IL12B risk haplotype and lack of interaction with HLA-Cw6 among the psoriasis patients in India - صفحه:389-395 Comparison between CaGene 5.1 and 6.0 for BRCA1/2 mutation prediction: a retrospective study of 150 BRCA1/2 genetic tests in 517 families with breast/ovarian cancer - صفحه:379-387 Comparison of exome-based HLA class I genotyping tools: identification of platform-specific genotyping errors - صفحه:397-405 Gender-dependent and age-of-onset-specific association of the rs11675434 single-nucleotide polymorphism near TPO with susceptibility to Graves’ ophthalmopathy - صفحه:373-377 Genetic trail for the early migrations of Aisin Gioro, the imperial house of the Qing dynasty - صفحه:407-411 Genotype and phenotype characterization in a Spanish cohort with isovaleric acidemia - صفحه:355-360 HMSN Lom in 12 Czech patients, with one unusual case due to uniparental isodisomy of chromosome 8 - صفحه:431-435 Identification of a novel LRRK1 mutation in a family with osteosclerotic metaphyseal dysplasia - صفحه:437-441 Late-onset episodic ataxia associated with SLC1A3 mutation - صفحه:443-446 Mitochondrial DNA diversity of present-day Aboriginal Australians and implications for human evolution in Oceania - صفحه:343-353 Novel and recurrent XYLT1 mutations in two Turkish families with Desbuquois dysplasia, type 2 - صفحه:447-451 Phylogenetic and population-based approaches to mitogenome variation do not support association with male infertility - صفحه:361-371 The investigation of the origin of Southern Tunisians using HLA genes - صفحه:419-429