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The -9247 T/C polymorphism in the SOST upstream regulatory region that potentially affects C/EBPalpha and FOXA1 binding is associated with osteoporosis.
Development and evaluation of a PCR and mass spectroscopy (PCR-MS)-based method for quantitative, type-specific detection of human papillomavirus.
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.
The role of cell-free circulating DNA in the diagnosis and prognosis of prostate cancer
Sequenom MassARRAY application in the long QT syndromeÂ mutation detection
Non-invasive prenatal diagnosis using cell-free fetal DNA in maternal plasma from PGD pregnancies
Genetic association analysis of LARS2 with type 2 diabetes.
A Variant of the SLC10A2 Gene Encoding the Apical Sodium-Dependent Bile Acid Transporter Is a Risk Factor for Gallstone Disease
A single-nucleotide polymorphism of the TNFAIP3 gene is associated with systemic lupus erythematosus in Chinese Han population
IL7RA polymorphisms and chronic inflammatory arthropathies.