High-resolution array CGH defines critical regions and candidate genes for microcephaly, abnormalities of the corpus callosum, and seizure phenotypes in patients with microdeletions of 1q43q44

✍ Scribed by Blake C. Ballif; Jill A. Rosenfeld; Ryan Traylor; Aaron Theisen; Patricia I. Bader; Roger L. Ladda; Susan L. Sell; Michelle Steinraths; Urvashi Surti; Marianne McGuire; Shelley Williams; Sandra A. Farrell; James Filiano; Rhonda E. Schnur; Lauren B. Coffey; Raymond C. Tervo; Tracy Stroud; Michael Marble; Michael Netzloff; Kristen Hanson; Arthur S. Aylsworth; J. S. Bamforth; Deepti Babu; Dmitriy M. Niyazov; J. Britt Ravnan; Roger A. Schultz; Allen N. Lamb; Beth S. Torchia; Bassem A. Bejjani; Lisa G. Shaffer

• Book ID: 106135194
• Publisher: Springer
• Year: 2011
• Tongue: English
• Weight: 771 KB
• Volume: 131
• Category: Article
• ISSN: 0340-6717
• DOI: 10.1007/s00439-011-1073-y