## Abstract Using aCGH, we have identified a pericentromeric deletion, spanning about 8.2 Mb, within 16p11.2–p12.2 in a patient with developmental delay (DD) and dysmorphic features. This deletion arose de novo and is flanked by segmental duplications. The proposita was the only child of healthy no
✦ LIBER ✦
Microdeletion syndrome 16p11.2-p12.2: Clinical and molecular characterization
✍ Scribed by Maja Hempel; Nuria Rivera Brugués; Janine Wagenstaller; Gaby Lederer; Andrea Weitensteiner; Heide Seidel; Thomas Meitinger; Tim M. Strom
- Publisher
- John Wiley and Sons
- Year
- 2009
- Tongue
- English
- Weight
- 166 KB
- Volume
- 149A
- Category
- Article
- ISSN
- 1552-4825
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