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Search Results for: Hereditary Genetics
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Association study of a new schizophrenia susceptibility locus of 10q24.32-33 in a Han Chinese population
The rs9509 polymorphism of MMP-9 is associated with risk of hemorrhage in brain arteriovenous malformations
Association of PTEN genetic polymorphisms with atherosclerotic cerebral infarction in the Han Chinese population
PRM1 variant rs35576928 (Arg>Ser) is associated with defective spermatogenesis in the Chinese Han population
Association of single nucleotide polymorphisms in the genes ATM, GSTP1, SOD2, TGFB1, XPD and XRCC1 with risk of severe erythema after breast conserving radiotherapy
Rare and Common Variants in CARD14, Encoding an Epidermal Regulator of NF-kappaB, in Psoriasis
Polymorphisms in the glutamate decarboxylase 1 gene associated with heroin dependence
Detection of pathogenic mutations and the mechanism of a rare chromosomal rearrangement in a Chinese family with Becker muscular dystrophy
Glaucoma Risk Alleles at CDKN2B-AS1 Are Associated with Lower Intraocular Pressure, Normal-Tension Glaucoma, and Advanced Glaucoma
Association between polymorphisms in cytokine genes IL-17A and IL-17F and development of allergic rhinitis and comorbid asthma in Chinese subjects
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