Exome sequencing identifies ZFPM2 as a cause of familial isolated congenital diaphragmatic hernia and possibly cardiovascular malformations

✍ Scribed by Brady, Paul D.; Van Houdt, Jeroen; Callewaert, Bert; Deprest, Jan; Devriendt, Koenraad; Vermeesch, Joris R.

• Book ID: 121826931
• Publisher: Elsevier Science
• Year: 2014
• Tongue: English
• Weight: 476 KB
• Volume: 57
• Category: Article
• ISSN: 1769-7212
• DOI: 10.1016/j.ejmg.2014.04.006