Interstitial deletion 1q42 in a patient with agenesis of corpus callosum: Phenotype–genotype comparison to the 1q41q42 microdeletion suggests a contiguous 1q4 syndrome

✍ Scribed by Isabel Filges; Benno Röthlisberger; Nemya Boesch; Peter Weber; Friedel Wenzel; Andreas R. Huber; Karl Heinimann; Peter Miny

• Publisher: John Wiley and Sons
• Year: 2010
• Tongue: English
• Weight: 231 KB
• Volume: 152A
• Category: Article
• ISSN: 1552-4825
• DOI: 10.1002/ajmg.a.33330