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journal of human genetics
سال:2015 - دوره:60 - شماره:2
A powerful association test for qualitative traits incorporating imprinting effects using general pedigree data
- صفحه:77-83
Deep sequencing of RYR3 gene identifies rare and common variants associated with increased carotid intima-media thickness (cIMT) in HIV-infected individuals
- صفحه:63-67
Downregulation of the microRNA-1/133a cluster enhances cancer cell migration and invasion in lung-squamous cell carcinoma via regulation of Coronin1C
- صفحه:53-61
Erratum: An A/C germline single-nucleotide polymorphism in the TNFAIP3 gene is associated with advanced disease stage and survival in only surgically treated esophageal cancer
- صفحه:107-107
Genetic structure among Fijian island populations
- صفحه:69-75
Mutations in the glucocerebrosidase gene are responsible for Chinese patients with Parkinson’s disease
- صفحه:85-90
Mutations in the glutaminyl-tRNA synthetase gene cause early-onset epileptic encephalopathy
- صفحه:97-101
Severe phenotypes in a Charcot–Marie–Tooth 1A patient with PMP22 triplication
- صفحه:103-106
Silver–Russell syndrome without body asymmetry in three patients with duplications of maternally derived chromosome 11p15 involving CDKN1C
- صفحه:91-95
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