Maternal Folate Polymorphisms and the Etiology of Human Nondisjunction
- 1 August 2001
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 69 (2) , 434-439
- https://doi.org/10.1086/321971
Abstract
No abstract availableKeywords
This publication has 17 references indexed in Scilit:
- Methylenetetrahydrofolate Reductase Polymorphism in the Etiology of Down SyndromePediatric Research, 2002
- MTRR and MTHFR polymorphism: Link to Down syndrome?American Journal of Medical Genetics, 2001
- Maternal sex chromosome non-disjunction: evidence for X chromosome-specific risk factorsHuman Molecular Genetics, 2001
- 5, 10-Methylenetetrahydrofolate Reductase Gene Variants and Congenital Anomalies: A HuGE ReviewAmerican Journal of Epidemiology, 2000
- Abnormal folate metabolism and mutation in the methylenetetrahydrofolate reductase gene may be maternal risk factors for Down syndromeThe American Journal of Clinical Nutrition, 1999
- Nondisjunction of human acrocentric chromosomes: studies of 432 trisomic fetuses and livebornsHuman Genetics, 1994
- The origin of 47, XXY and 47, XXX aneuploidy: heterogeneous mechanisms and role of aberrant recombinationHuman Molecular Genetics, 1994
- Molecular studies of trisomy 18.1993
- Maternal age-specific rates of numerical chromosome abnormalities with special reference to trisomyHuman Genetics, 1985
- A cytogenetic study of 1000 spontaneous abortionsAnnals of Human Genetics, 1980