- Title
- Maternal folate polymorphisms and the etiology of human nondisjunction
- Creators
- Terry J HASSOLD - Department of Genetics and The Center for Human Genetics, Case Western Reserve University and University Hospitals of Cleveland, Cleveland, United StatesLindsay C BURRAGE - Department of Genetics and The Center for Human Genetics, Case Western Reserve University and University Hospitals of Cleveland, Cleveland, United StatesErnest R CHAN - Department of Genetics and The Center for Human Genetics, Case Western Reserve University and University Hospitals of Cleveland, Cleveland, United StatesLuann M JUDIS - Department of Genetics and The Center for Human Genetics, Case Western Reserve University and University Hospitals of Cleveland, Cleveland, United StatesStuart SCHWARTZ - Department of Genetics and The Center for Human Genetics, Case Western Reserve University and University Hospitals of Cleveland, Cleveland, United StatesS JILL JAMES - Division of Biochemical Toxicology, Food and Drug Administration-National Center for Toxicological Research, Jefferson, AR, United StatesPatricia A JACOBS - Wessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, Wiltshire, Salisbury, United KingdomN SIMON THOMAS - Wessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, Wiltshire, Salisbury, United Kingdom
- Publication Details
- American journal of human genetics, Vol.69(2), pp.434-439
- Academic Unit
- Molecular Biosciences, School of
- Publisher
- University of Chicago Press; Chicago, IL
- Identifiers
- 99900547443901842
- Language
- English
- Resource Type
- Journal article
Journal article
Maternal folate polymorphisms and the etiology of human nondisjunction
American journal of human genetics, Vol.69(2), pp.434-439
2001
Handle:
https://hdl.handle.net/2376/112915
PMCID: PMC1235315
PMID: 11443546
Abstract
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