Clinical and molecular characterization of two patients with a 6.75 Mb overlapping deletion in 8p12p21 with two candidate loci for congenital heart defects

✍ Scribed by Marjolein H. Willemsen; Nicole de Leeuw; Rolph Pfundt; Bert B.A. de Vries; Tjitske Kleefstra

• Book ID: 116433170
• Publisher: Elsevier Science
• Year: 2009
• Tongue: English
• Weight: 390 KB
• Volume: 52
• Category: Article
• ISSN: 1769-7212
• DOI: 10.1016/j.ejmg.2009.03.003