Genetic Factors in Congenital Diaphragmatic Hernia
Authors:
- A.M. HolderAHA.M. Holder
- M. KlaassensMKM. Klaassens
- D. TibboelDTD. Tibboel
- A. de KleinAKA. de Klein
- B. LeeBLB. Lee
- D.A. ScottDSD.A. Scott
- 1 May 2007
- journal article
- review article
- Published by Elsevier in The American Journal of Human Genetics
- Vol. 80 (5) , 825-845
Abstract
No abstract availableKeywords
This publication has 177 references indexed in Scilit:
- Impaired mesenchymal cell function in Gata4 mutant mice leads to diaphragmatic hernias and primary lung defectsDevelopmental Biology, 2007
- Hydrothorax in a patient with Denys-Drash syndrome associated with a diaphragmatic defectPediatric Nephrology, 2006
- Congenital diaphragmatic hernia associated with duplication of 11q23‐qterAmerican Journal of Medical Genetics Part A, 2006
- Congenital diaphragmatic hernia in a patient with tetrasomy 9pJournal of Pediatric Surgery, 2005
- Congenital Diaphragmatic Hernia and Chromosomal Anomalies: Autopsy StudyPediatric and Developmental Pathology, 2004
- GATA4 mutations cause human congenital heart defects and reveal an interaction with TBX5Nature, 2003
- Epidemiological study of congenital diaphragmatic defects with special reference to aetiologyEuropean Journal of Pediatrics, 1991
- Patterns of malformation in children with congenital diaphragmatic defectsThe Journal of Pediatrics, 1990
- Congenital posterolateral diaphragmatic hernia: Associated malformationsJournal of Pediatric Surgery, 1988
- Congenital diaphragmatic hernia: The hidden mortalityJournal of Pediatric Surgery, 1978