Expanding diagnostic testing beyond cytogenetics: Implications for birth defects research and surveillance-Reference-Cited by-同舟云学术

Expanding diagnostic testing beyond cytogenetics: Implications for birth defects research and surveillance

Published:2013-11 Issue:11 Volume:97 Page:726-729
ISSN:1542-0752
Container-title:Birth Defects Research Part A: Clinical and Molecular Teratology
language:en
Short-container-title:Birth Defects Research Part A: Clinical and Molecular Teratology

Author:

Jackson Jodi M.¹,Druschel Charlotte M.²,Shapira Stuart K.³

Affiliation:

1. Division of Birth Defects and Developmental Disabilities; National Center on Birth Defects and Developmental Disabilities, Centers for Disease Control and Prevention (CDC); Atlanta Georgia

2. New York State Congenital Malformations Registry; New York State Department of Health; Troy New York

3. Office of the Director, National Center on Birth Defects and Developmental Disabilities; Centers for Disease Control and Prevention (CDC); Atlanta Georgia

Publisher

Wiley

Subject

Developmental Biology,Embryology,General Medicine,Pediatrics, Perinatology, and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/bdra.23195/fullpdf

Reference44 articles.

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3. A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population;Botto;Pediatrics,2003

4. Retrospective and prospective epidemiological studies of 1500 karyotyped spontaneous human abortions;Boué;Teratology,1975

5. Q-banding of chromosomes in human spontaneous abortions;Carr;Can J Genet Cytol,1978

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