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Involvement of hypertrophic cardiomyopathy genes in sudden infant death syndrome (SID)
The -9247 T/C polymorphism in the SOST upstream regulatory region that potentially affects C/EBPalpha and FOXA1 binding is associated with osteoporosis.
GATA-2 L359 V mutation is exclusively associated with CML progression but not other hematological malignancies and GATA-2 P250A is a novel single nucleotide polymorphism.
Sequenom MassARRAY application in the long QT syndromeÂ mutation detection
Genetic association analysis of LARS2 with type 2 diabetes.
A single-nucleotide polymorphism of the TNFAIP3 gene is associated with systemic lupus erythematosus in Chinese Han population
A genetic variant of G6PC2 is associated with type 2 diabetes and fasting plasma glucose level in the Chinese population
TNF superfamily gene polymorphism as prognostic factor in early breast cancer
A Variant of the SLC10A2 Gene Encoding the Apical Sodium-Dependent Bile Acid Transporter Is a Risk Factor for Gallstone Disease
rs5888 variant of SCARB1 gene is a possible susceptibility factor for age-related macular degeneration