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journal of human genetics
سال:2017 - دوره:62 - شماره:12
A genome-wide association analysis identifies NMNAT2 and HCP5 as susceptibility loci for Kawasaki disease
- صفحه:1023-1029
Effect of GnRHR polymorphisms on in vitro fertilization and embryo transfer in patients with polycystic ovary syndrome
- صفحه:1065-1071
Pathogen lineage-based genome-wide association study identified CD53 as susceptible locus in tuberculosis
- صفحه:1015-1022
Population-based biobank participants’ preferences for receiving genetic test results
- صفحه:1037-1048
Precise mapping of 17 deletion breakpoints within the central hotspot deletion region (introns 50 and 51) of the DMD gene
- صفحه:1057-1063
Santos syndrome is caused by mutation in the WNT7A gene
- صفحه:1073-1078
Shared genetic variants for polypoidal choroidal vasculopathy and typical neovascular age-related macular degeneration in East Asians
- صفحه:1049-1055
Skewed X inactivation in Lesch–Nyhan disease carrier females
- صفحه:1079-1083
The 2017 JHG Young Scientist Award
- صفحه:1007-1007
The clinical characteristics of Asian patients with classical-type Hutchinson–Gilford progeria syndrome
- صفحه:1031-1035
The pharmacogenomics of valproic acid
- صفحه:1009-1014
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