Characterization of the chromosome 1q41q42.12 region, and the candidate gene DISP1, in patients with CDH-Reference-Cited by-同舟云学术

Characterization of the chromosome 1q41q42.12 region, and the candidate gene DISP1, in patients with CDH

Published:2010-08-26 Issue:10 Volume:152A Page:2493-2504
ISSN:1552-4825
Container-title:American Journal of Medical Genetics Part A
language:en
Short-container-title:Am. J. Med. Genet.

Author:

Kantarci Sibel,Ackerman Kate G.,Russell Meaghan K.,Longoni Mauro,Sougnez Carrie,Noonan Kristin M.,Hatchwell Eli,Zhang Xiaoyun,Vanmarcke Rafael Pieretti,Anyane-Yeboa Kwame,Dickman Paul,Wilson Jay,Donahoe Patricia K.,Pober Barbara R.

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Reference43 articles.

1. Fog2 is required for normal diaphragm and lung development in mice and humans;Ackerman;PLoS Genet,2005

2. Pathogenesis of nitrofen-induced congenital diaphragmatic hernia in fetal rats;Allan;J Appl Physiol,1997

3. Coexisting congenital diaphragmatic hernia, esophageal atresia, and tracheoesophageal fistula: A case report and review of the literature;Al-Salem;Int Surg,2008

4. Embryological origins and development of the rat diaphragm;Babiuk;J Comp Neurol,2003

5. Structural and functional characterization of the mouse Hlx homeobox gene;Bates;Mamm Genome,2000

Cited by 50 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Prenatal Ultrasound Diagnosis of Congenital Diaphragmatic Hernia in a Fetus With Fryns “Anophthalmia-Plus” Syndrome: A Case Report;Cureus;2024-08-28

2. Frem1 activity is regulated by Sonic hedgehog signaling in the cranial neural crest mesenchyme during midfacial morphogenesis;Developmental Dynamics;2022-12-19

3. Frem1 activity regulated by Sonic Hedgehog signaling in the cranial neural crest mesenchyme guides midfacial morphogenesis;2022-07-18

4. Molecular Mechanisms Contributing to the Etiology of Congenital Diaphragmatic Hernia: A Review and Novel Cases;The Journal of Pediatrics;2022-07

5. Two Novel Variants of WDR26 in Chinese Patients with Intellectual Disability;Genes;2022-05-02