Absence of association of fetal MTHFR C677T polymorphism with prenatal Down syndrome pregnancies [2]

European Journal of Human Genetics

Volumn 11, Issue 1, 2003, Pages 5-

  Yanamandra, Krishna ^a   Bocchini Jr , Joseph A ^a   Thurmon, Theodore F ^a  

^a Louisiana State University School of Medicine Shreveport   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2);

ALLELE; CAUCASIAN; CHROMOSOME ABERRATION; CLINICAL ARTICLE; CONTROLLED STUDY; CORRELATION ANALYSIS; DOWN SYNDROME; FREQUENCY ANALYSIS; GENE MUTATION; GENETIC POLYMORPHISM; GENETIC RISK; GENOTYPE; HOMOZYGOSITY; HUMAN; INFANT; KARYOTYPE; LETTER; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; RISK ASSESSMENT; TRISOMY 21;

DOWN SYNDROME; EUROPEAN CONTINENTAL ANCESTRY GROUP; FEMALE; FETAL DISEASES; HOMOZYGOTE; HUMANS; METHYLENETETRAHYDROFOLATE REDUCTASE (NADPH2); OXIDOREDUCTASES ACTING ON CH-NH GROUP DONORS; POLYMORPHISM, GENETIC; PREGNANCY;

EID: 0037269142     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5200928     Document Type: Letter

References (2)

1. Stuppia L, Gatta V, Gaspari AR et al: C677T mutation in the 5, 10-MTHFR gene and risk of Down syndrome in Italy. Eur J Hum Genet 2002; 10: 388-390.
2. Yanamandra K, Gadi I, Napper D, Chen H, Bocchini Jr JA, Thurmon TF, Dhanireddy R: MTHFR C677T polymorphism in pregnancies with Chromosomal Defects. Amer J Hum Genet 2001; 69: 431.