Molecular characterization of del(8)(p23.1p23.1) in a case of congenital diaphragmatic hernia-Reference-Cited by-同舟云学术

Molecular characterization of del(8)(p23.1p23.1) in a case of congenital diaphragmatic hernia

Published:2005 Issue:1 Volume:136A Page:49-51
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Shimokawa Osamu,Miyake Noriko,Yoshimura Takazumi,Sosonkina Nadiya,Harada Naoki,Mizuguchi Takeshi,Kondoh Shinji,Kishino Tatsuya,Ohta Tohru,Remco Visser,Takashima Takeshi,Kinoshita Akira,Yoshiura Koichiro,Niikawa Norio,Matsumoto Naomichi

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference13 articles.

1. Congenital Diaphragmatic Hernia and Chromosomal Anomalies: Autopsy Study

2. Delineation of the Critical Deletion Region for Congenital Heart Defects, on Chromosome 8p23.1

3. Prenatal diagnosis of an 8p23.1 deletion in a fetus with a diaphragmatic hernia and review of the literature

4. GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5

5. Olfactory Receptor–Gene Clusters, Genomic-Inversion Polymorphisms, and Common Chromosome Rearrangements

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