Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

✍ Scribed by Quaderi, Nandita A.; Schweiger, Susann; Gaudenz, Karin; Franco, Brunella; Rugarli, Elena I.; Berger, Wolfgang; Feldman, George J.; Volta, Manuela; Andolfi, Grazia; Gilgenkrantz, S.

• Book ID: 109918654
• Publisher: Nature Publishing Group
• Year: 1997
• Tongue: English
• Weight: 880 KB
• Volume: 17
• Category: Article
• ISSN: 1061-4036
• DOI: 10.1038/ng1197-285