Publications by authors named "S Chatkupt"

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New 19 bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR): a risk factor for spina bifida acting in mothers during pregnancy?
William G Johnson, Edward S Stenroos, John R Spychala, Sansnee Chatkupt, Sue X Ming

Am J Med Genet A· February 2004

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Distribution of alleles of the methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism in familial spina bifida.
W G Johnson, E S Stenroos, S C Heath, Y Chen, R Carroll, S Chatkupt

Am J Med Genet· December 1999

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Clinical manifestations of mitochondrial DNA depletion.
T H Vu, M Sciacco, K Tanji, C Nichter, E Bonilla, S Chatkupt

Neurology· June 1998

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Dejerine-Sottas neuropathy in mother and son with same point mutation of PMP22 gene.
V V Ionasescu, C C Searby, R Ionasescu, S Chatkupt, N Patel

Muscle Nerve· January 1997

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PAX genes and human neural tube defects: an amino acid substitution in PAX1 in a patient with spina bifida.
F A Hol, M P Geurds, S Chatkupt, Y Y Shugart, R Balling

J Med Genet· August 1996

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