Genetic Variants in the Methylenetetrahydrofolate Reductase Gene in Egyptian Children with Conotruncal Heart Defects and their Mothers
Author:
Publisher
Scientific Foundation SPIROSKI
Subject
General Medicine
Link
http://versita.metapress.com/index/DHQJU5W8VP18N524.pdf
Cited by 5 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 between MTHFR C677T variant and risk for congenital heart defects in Egyptian children: a case–control study including meta-analysis based on 147 cases and 143 controls;Egyptian Journal of Medical Human Genetics;2023-04-03
2. “Association of MTHFR and MS/MTR gene polymorphisms with congenital heart defects in North Indian population (Jammu and Kashmir): a case–control study encompassing meta-analysis and trial sequential analysis”;BMC Pediatrics;2022-04-25
3. Are polymorphisms in MTRR A66G and MTHFR C677T genes associated with congenital heart diseases in Iranian population?;CASP J INTERN MED;2017
4. Association of MTHFR A1298C polymorphism with conotruncal heart disease;Cardiology in the Young;2014-12-30
5. MTHFR C677T and A1298C gene polymorphisms and their relation to homocysteine level in Egyptian children with congenital heart diseases;Gene;2013-10
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