Human Genome Epidemiology Literature Finder
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Records 1 - 6 (of 6 Records) |
| Query Trace: Tetralogy of Fallot and MTHFR[original query] |
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| Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases. Acta obstetricia et gynecologica Scandinavica 2005 Dec 84 (12): 1134-40. Lee Chien-Nan, Su Yi-Ning, Cheng Wen-Fang, Lin Ming-Tai, Wang Jou-Kou, Wu Mei-Hwan, Hsieh Fon-J |
| The methylenetetrahydrofolate reductase gene variant (C677T) as a susceptibility gene for tetralogy of Fallot. Revista portuguesa de cardiologia : orgão oficial da Sociedade Portuguesa de Cardiologia = Portuguese journal of cardiology : an official journal of the Portuguese Society of Cardiology 0 28 (7-8): 809-12. Marinho Cláudia, Alho Irina, Guerra António, Rego Carla, Areias José, Bicho Manu |
| Methylenetetrahydrofolate reductase C677T and reduced folate carrier 80 G>A polymorphisms are associated with an increased risk of conotruncal heart defects. Clinical chemistry and laboratory medicine : CCLM / FESCC 2012 Aug 50 (8): 1455-61. Gong Dingxu, Gu Haiyong, Zhang YuJian, Gong Jie, Nie Yu, Wang Jue, Zhang Hui, Liu Ruiping, Hu Shengshou, Zhang H |
| MTHFR rs1801133 C>T polymorphism is associated with an increased risk of tetralogy of Fallot. Biomedical reports 2014 Mar 2 (2): 172-176. Huang Jianbing, Mei Ju, Jiang Lianyong, Jiang Zhaolei, Liu Hao, Ding Fangb |
| Are polymorphisms in MTRR A66G and MTHFR C677T genes associated with congenital heart diseases in Iranian population? Caspian journal of internal medicine 2017 8 (2): 83-90. Noori Noormohammad, Miri-Moghaddam Ebrahim, Dejkam Asieh, Garmie Yasman, Bazi A |
| Association between 5,10-methylenetetrahydrofolate, gene polymorphism and congenital heart disease. Journal of biological regulators and homeostatic agents 0 32 (5): 1255-1260. Wang H L, Sun L, Zhou S, Wang |
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