Analysis of MTHFR and MTRR Gene Polymorphisms in Iranian Ventricular Septal Defect Subjects

118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects

(2009) Gary M Shaw et al.   BMC Medical Genetics

Genetic and environmental influences on total plasma homocysteine and coronary artery disease (CAD) risk among South Indians

(2009) Govindaiah Vinukonda et al.   CLINICA CHIMICA ACTA

Strengthening the reporting of genetic association studies (STREGA): an extension of the STROBE statement

(2009) Julian Little et al.   EUROPEAN JOURNAL OF EPIDEMIOLOGY

Methionine Synthase Reductase (MTRR) A66G polymorphism is not related to plasma homocysteine concentration and the risk for vascular disease

(2009) C. Scazzone et al.   EXPERIMENTAL AND MOLECULAR PATHOLOGY

Screening NXK2.5 Mutation in a Sample of 230 Han Chinese Children with Congenital Heart Diseases

(2009) Weimin Zhang et al.   Genetic Testing and Molecular Biomarkers

The Association Between Common C677T Mutation in Methylenetetrahydrofolate Reductase Gene and the Risk of Venous Thrombosis in an Iranian Population

(2008) Mohammad Soleyman Soltanpour et al.   Labmedicine

Genetic and lifestyle factors related to the periconception vitamin B12 status and congenital heart defects: A Dutch case-control study

(2008) Anna C. Verkleij-Hagoort et al.   MOLECULAR GENETICS AND METABOLISM