Molecular characterization of Beckwith-Wiedemann syndrome (BWS) patients with partial duplication of chromosome 11p excludes the gene MYOD1 from the BWS region

✍ Scribed by Weksberg, R.; Glaves, M.; Teshima, I.; Waziri, M.; Patil, S.; Williams, B.R.G.

• Book ID: 122731740
• Publisher: Elsevier Science
• Year: 1990
• Tongue: English
• Weight: 796 KB
• Volume: 8
• Category: Article
• ISSN: 0888-7543
• DOI: 10.1016/0888-7543(90)90256-T