| 1 | MTRR, NTDS1
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| Altered folate metabolism and disposition in mothers affected by a spina bifida pregnancy: influence of 677c --> t methylenetetrahydrofolate reductase and 2756a --> g methionine synthase genotypes.
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| Lucock M, Daskalakis I, Briggs D, Yates Z, Levene M.
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| Mol Genet Metab 70(1):27-44. 2000
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| 2 | MTRR, NTDS1
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| Investigation of folate pathway gene polymorphisms and the incidence of neural tube defects in a Texas hispanic population.
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| Barber R, Shalat S, Hendricks K, Joggerst B, Larsen R, Suarez L, Finnell R.
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| Mol Genet Metab 70(1):45-52. 2000
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| 3 | MTHFR, NTDS1
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| The Thermolabile Variant of Methylenetetrahydrofolate Reductase and Neural Tube Defects: An Evaluation of Genetic Risk and the Relative Importance of the Genotypes of the Embryo and the Mother.
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| Shields DC, et al.
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| Am J Hum Genet 64(4):1045-1055. 1999
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| 4 | NTDS1, MTHFR
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| Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects.
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| Christensen B, et al.
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| Am J Med Genet 84(2):151-7. 1999
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| 5 | MTHFR, NTDS1
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| High prevalence of the thermolabile methylenetetrahydrofolate reductase variant in mexico: A country with a very high prevalence of neural tube defects.
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| Mutchinick OM, Lopez MA, Luna L, Waxman J, Babinsky VE.
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| Mol Genet Metab 68(4):461-7 1999
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| 6 | MTHFR, NTDS1
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| A second common mutation in the methylenetetrahydrofolate reductase gene : an additional risk factor for neural-tube defects?
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| van der Put NMJ, et al.
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| Am J Hum Genet 62 : 1044-1051. 1998
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| 7 | MTHFR, NTDS1
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| Evaluation of the MTHFR C677T allele and the MTHFR gene locus in a German spina bifida population.
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| Koch MC, et al.
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| Eur J Pediatr 157 : 487-492. 1998
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| 8 | MTHFR, NTDS1
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| The C677T mutation of the 5,10-methylenetetrahydrofolate reductase gene is a moderate risk factor for spina bifida in Italy.
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| De Franchis R, et al.
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| J Med Genet 35 : 1009-1013. 1998
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| 9 | BRCA1, CBS, MTHFR, MTR, NTDS1, T
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| Susceptibility to spina bifida : an association study of five candidate genes.
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| Morrison K, et al.
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| Ann Hum Genet 62 : 379-396. 1998
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