Terminal 6.9 Mb deletion of chromosome 15q, associated with a structurally abnormal X chromosome in a patient with congenital diaphragmatic hernia and heart defect

✍ Scribed by Sylvie Jaillard; Philippe Loget; Josette Lucas; Christèle Dubourg; Gwenaelle Le Bouar; Florence Demurger; Isabelle Bertorello; Véronique David; Patrice Poulain; Sylvie Odent; Marc-Antoine Belaud-Rotureau

• Book ID: 116433333
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 415 KB
• Volume: 54
• Category: Article
• ISSN: 1769-7212
• DOI: 10.1016/j.ejmg.2010.11.001