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Search Results for: Hereditary Genetics
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Candidate loci for insulin sensitivity and disposition index from a genome-wide association analysis of Hispanic participants in the Insulin Resistance Artherosclerosis (IRAS) family study
Association of genetic variations of NOS1AP with type 2 diabetes in a Chinese population
Novel quantitative trait loci for central corneal thickness identified by candidate gene analysis of osteogenesis imperfecta genes
Polymorphisms in surfactant protein D are associated with COPD
SNCA Variant Associated With Parkinson Disease and Plasma {alpha}-Synuclein Level
Association of α-, β-, and γ–synuclein with diffuse Lewy body disease
Association of IL1A, IL1B, and TNF gene polymorphisms with chronic rhinosinusitis with and without nasal polyposis
Association of genetic variants in the neurotrophic receptor-encoding gene NTRK2 and a lifetime history of suicide attempts in depressed patients
Association of STAT3 and TNFRSF1A with ankylosing spondylitis in Han Chinese
The -9247 T/C polymorphism in the SOST upstream regulatory region that potentially affects C/EBPalpha and FOXA1 binding is associated with osteoporosis.
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