Study of the origin of nondisjunction in a family with two cases of Down syndrome using cytogenetic and molecular polymorphisms-Reference-Cited by-同舟云学术

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Study of the origin of nondisjunction in a family with two cases of Down syndrome using cytogenetic and molecular polymorphisms

Published:2005-06-03 Issue:S7 Volume:37 Page:133-136
ISSN:0148-7299
Container-title:American Journal of Medical Genetics
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Stinissen Piet,Van Roy Bernadette,Van Camp Guy,Backhovens Hubert,Partoens Peter,Wehnert Anita,Verniers Heidi,Dumon Jan,Vandenberghe Antoon,Van Broeckhoven Christine

Publisher

Wiley

Subject

Genetics(clinical)

Reference22 articles.

1. Evidence for genetic control of nondisjunction in man;Alfi;Am J Hum Genet,1980

2. Analysis of DNA haplotypes suggest a genetic predisposition to trisomy 21 associated with DNA sequences on chromosome 21;Antonarakis;Proc Natl Acad Sci USA,1985

3. Report of the committee on the genecic constitution of chromosomes 20, 21 and 22. HGM 9. 5;Carritt;Cytogenet Cell Genet,1988

4. Use of a chromosome 21 cloned DNA probe for the analysis of nondisjunction in Down synbdrome;Davies;Hum Genet,1984

5. Partial physical map of Human chromosome 21;Gardiner;Somatic Cell Mol Genet,1988

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