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journal of human genetics
سال:2016 - دوره:61 - شماره:12
A survey on awareness of genetic counseling for non-invasive prenatal testing: the first year experience in Japan
- صفحه:995-1001
Co-stimulatory CD28 and transcription factor NFKB1 gene variants affect idiopathic recurrent miscarriages
- صفحه:1035-1041
FKRP mutations, including a founder mutation, cause phenotype variability in Chinese patients with dystroglycanopathies
- صفحه:1013-1020
Frontotemporal dementia-related gene mutations in clinical dementia patients from a Chinese population
- صفحه:1003-1008
Genetic-risk assessment of GWAS-derived susceptibility loci for type 2 diabetes in a 10 year follow-up of a population-based cohort study
- صفحه:1009-1012
Identification of novel susceptibility markers for the risk of overall breast cancer as well as subtypes defined by hormone receptor status in the Chinese population
- صفحه:1027-1034
Mitochondrial haplogroup M9a1a1c1b is associated with hypoxic adaptation in the Tibetans
- صفحه:1021-1026
Regulation of LOXL2 and SERPINH1 by antitumor microRNA-29a in lung cancer with idiopathic pulmonary fibrosis
- صفحه:985-993
Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis
- صفحه:977-984
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