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Search Results for: Hereditary Genetics

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  • Suboptimal maternal and cord plasma pyridoxal 5? phosphate concentrations are uncommon in a cohort of Canadian pregnant women and newborn infants
  • Sulfatase modifying factor 1 (SUMF1) is associated with Chronic Obstructive Pulmonary Disease
  • Targeted sequencing of ABCA7 identifies splicing, stop-gain and intronic risk variants for Alzheimer disease
  • TEX15: A DNA repair gene associated with prostate cancer risk in Han Chinese
  • The Association of Chemokine Gene Polymorphisms with VKH and Behcet’s Disease in a Chinese Han Population
  • The Association of SNP276G>T at Adiponectin Gene with Insulin Resistance and Circulating Adiponectin in Morbid Obese Patients After a Biliopancreatic Diversion Surgery
  • The association study of nonsyndromic cleft lip with or without cleft palate identified risk variants of the GLI3 gene in a Chinese population
  • The associations between VDR BsmI polymorphisms and risk of vitamin D deficiency, obesity and insulin resistance in adolescents residing in a tropical country
  • The contribution of CYP2C gene subfamily involved in epoxygenase pathway of arachidonic acids metabolism to hypertension susceptibility in Russian population
  • The effect of glucose-dependent insulinotropic polypeptide (GIP) variants on visceral fat accumulation in Han Chinese populations
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