journal of human genetics سال:2017 - دوره:62

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journal of human genetics
سال:2017 - دوره:62 - شماره:10

A common deletion in the haptoglobin gene associated with blood cholesterol levels among Chinese women - صفحه:911-914 Copy-number variants and candidate gene mutations in isolated split hand/foot malformation - صفحه:877-884 Deletions, not duplications or small mutations, are the predominante new mutations in the dystrophin gene - صفحه:885-888 Erratum: Corrigendum: Genetic diagnosis of Duchenne/Becker muscular dystrophy using next-generation sequencing: validation analysis of DMD mutations - صفحه:931-933 Inter-generational instability of inserted repeats during transmission in spinocerebellar ataxia type 31 - صفحه:923-925 Maternally derived 15q11.2-q13.1 duplication and H19 -DMR hypomethylation in a patient with Silver–Russell syndrome - صفحه:919-922 Meta-analysis of genome-wide SNP- and pathway-based associations for facets of neuroticism - صفحه:903-909 Moving towards successful exon-skipping therapy for Duchenne muscular dystrophy - صفحه:871-876 Phylogeny of Y-chromosome haplogroup C3b-F1756, an important paternal lineage in Altaic-speaking populations - صفحه:915-918 Replication and fine-mapping of genetic predictors of lipid traits in African–Americans - صفحه:895-901 Siblings with optic neuropathy and RTN4IP1 mutation - صفحه:927-929 al mena: a comprehensive resource of human genetic variants integrating genomes and exomes from Arab, Middle Eastern and North African populations - صفحه:889-894