Human Genome Epidemiology Literature Finder
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Query Trace: Neural Tube Defects and COMT[original query] |
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Catechol-O-methyltransferase genotype is associated with plasma total homocysteine levels and may increase venous thrombosis risk. Thrombosis and haemostasis 2007 Dec 98 (6): 1226-31. Gellekink Henkjan, Muntjewerff Jan-Willem, Vermeulen Sita H H M, Hermus Ad R M M, Blom Henk J, den Heijer Mart |
Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study population. American journal of medical genetics. Part A 2011 Jan 155A (1): 14-21. Carter Tonia C, Pangilinan Faith, Troendle James F, Molloy Anne M, VanderMeer Julia, Mitchell Adam, Kirke Peadar N, Conley Mary R, Shane Barry, Scott John M, Brody Lawrence C, Mills James |
Variants in maternal COMT and MTHFR genes and risk of neural tube defects in offspring. Metabolic brain disease 2015 Apr 30 (2): 507-13. Liu Jufen, Zhang Yali, Jin Lei, Li Guoxing, Wang Linlin, Bao Yanping, Fu Yunting, Li Zhiwen, Zhang Le, Ye Rongwei, Ren Aig |
Association between maternal COMT gene polymorphisms and fetal neural tube defects risk in a Chinese population. Birth defects research. Part A, Clinical and molecular teratology 2014 Jan 100 (1): 22-9. Liu Jufen, Wang Linlin, Fu Yunting, Li Zhiwen, Zhang Yali, Zhang Le, Jin Lei, Ye Rongwei, Ren Aig |
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