A de novo 1.1 Mb microdeletion of chromosome 19p13.11 provides indirect evidence for EPS15L1 to be a strong candidate for split hand split foot malformation

✍ Scribed by Susanne Bens; Andrea Haake; Holger Tönnies; Inga Vater; Ulrich Stephani; Paul-Martin Holterhus; Reiner Siebert; Almuth Caliebe

• Book ID: 116433400
• Publisher: Elsevier Science
• Year: 2011
• Tongue: English
• Weight: 758 KB
• Volume: 54
• Category: Article
• ISSN: 1769-7212
• DOI: 10.1016/j.ejmg.2011.05.004