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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jun 7, 2023. (Total: 217722Documents)
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Records 1 - 3 (of 3 Records)

Query Trace: Meningomyelocele and MTHFR[original query]
The effect of C677T mutation of methylene tetrahydrofolate reductase gene and plasma folate level on hyperhomocysteinemia in patients with meningomyelocele.
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery 2000 Sep 16 (9): 559-63.
Lee B H, Cheong H I, Shin Y S, Cho B K, Wang K
Role of parental folate pathway single nucleotide polymorphisms in altering the susceptibility to neural tube defects in South India.
Journal of perinatal medicine 2010 38 (1): 63-9.
Naushad Shaik Mohammad, Devi Akella Radha Ra
Metabolic Analysis of Methylenetetrahydrofolate Reductase Single Nucleotide Polymorphisms (MTHFR 677C<T and MTHFR 1298A<C), Serum Folate and Vitamin B12 in Neural Tube Defects.
Indian journal of clinical biochemistry : IJCB 2023 5 38 (3): 305-315.
Mohammed H Hassan, Mohamed A Raslan, Mena Tharwat, Hala M Sakhr, Eslam El-Sayed El-Khateeb, Shimaa Fathy Sakr, Hesham H Ameen, Ali R Hamd
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