677right-arrowCT mutation on the methylenetetrahydrofolate reductase gene is not a risk factor for neural tube defects in Turkey
Author:
Publisher
BMJ
Subject
Obstetrics and Gynecology,General Medicine,Pediatrics, Perinatology and Child Health
Cited by 15 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. Association of Polymorphism of the Methyl Tetrahydrofolate Reductase (MTHFR) Gene with Anti-Seizure Medication Response in Pediatric Patients in Jeddah, Saudi Arabia;Medicina;2022-11-03
2. Association betweenMTHFRC677T polymorphism and neural tube defect risks: A comprehensive evaluation in three groups of NTD patients, mothers, and fathers;Birth Defects Research Part A: Clinical and Molecular Teratology;2015-03-24
3. Case series of thromboembolic complications in childhood nephrotic syndrome: Hacettepe experience;Clinical and Experimental Nephrology;2014-07-04
4. PCMT1 gene polymorphisms, maternal folate metabolism, and neural tube defects: a case–control study in a population with relatively low folate intake;Genes & Nutrition;2013-08-06
5. Methylenetetrahydrofolate reductase C677T genetic polymorphisms and risk of leukaemia among the North Indian population;Cancer Epidemiology;2012-08
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