Deletion (1)(p32.2–p32.3) detected by array-CGH in a patient with developmental delay/mental retardation, dysmorphic features and low cholesterol: A new microdeletion syndrome?

✍ Scribed by Milene Mulatinho; Juan Llerena; Trond P. Leren; P. Nagesh Rao; Fabiola Quintero-Rivera

• Publisher: John Wiley and Sons
• Year: 2008
• Tongue: English
• Weight: 122 KB
• Volume: 146A
• Category: Article
• ISSN: 1552-4825
• DOI: 10.1002/ajmg.a.32454