Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia-Reference-Cited by-同舟云学术

Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia

Published:2009-07-15 Issue:8 Volume:149A Page:1661-1677
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Wat Margaret J.,Shchelochkov Oleg A.,Holder Ashley M.,Breman Amy M.,Dagli Aditi,Bacino Carlos,Scaglia Fernando,Zori Roberto T.,Cheung Sau Wai,Scott Daryl A.,Kang Sung-Hae Lee

Funder

NIH

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajmg.a.32896/fullpdf

Reference90 articles.

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3. Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH;Bi;Prenat Diagn,2008

4. Partial monosomy 8p with minimal dysmorphic signs;Blennow;J Med Genet,1990

5. Congenital diaphragmatic hernia and chromosomal anomalies: Autopsy study;Borys;Pediatr Dev Pathol,2004

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