journal of human genetics سال:2017 - دوره:62

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journal of human genetics
سال:2017 - دوره:62 - شماره:11

2SNP heritability and effects of genetic variants for neutrophil-to-lymphocyte and platelet-to-lymphocyte ratio - صفحه:979-988 A novel de novo mutation in CSNK2A1 : reinforcing the link to neurodevelopmental abnormalities and dysmorphic features - صفحه:1005-1006 An atypical case of SPG56/CYP2U1 -related spastic paraplegia presenting with delayed myelination - صفحه:997-1000 Association of autoimmune hepatitis with Src homology 2 adaptor protein 3 gene polymorphisms in Japanese patients - صفحه:963-967 Deep-intronic variant of fukutin is the most prevalent point mutation of Fukuyama congenital muscular dystrophy in Japan - صفحه:945-948 Genetic variants underlying vitamin D metabolism and VDR–TGFβ-1–SMAD3 interaction may impact on HCV progression: a study based on dbGaP data from the HALT-C study - صفحه:969-977 Genome-wide association study of neovascular age-related macular degeneration in the Thai population - صفحه:957-962 Postmortem genetic analysis of sudden unexpected death in infancy: neonatal genetic screening may enable the prevention of sudden infant death - صفحه:989-995 Regulation of SPOCK1 by dual strands of pre- miR-150 inhibit cancer cell migration and invasion in esophageal squamous cell carcinoma - صفحه:935-944 The absence that makes the difference: choroidal abnormalities in Legius syndrome - صفحه:1001-1004 The role of READ1 and KIAA0319 genetic variations in developmental dyslexia: testing main and interactive effects - صفحه:949-955