## Abstract Using aCGH, we have identified a pericentromeric deletion, spanning about 8.2 Mb, within 16p11.2βp12.2 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
The atypical 16p11.2 deletion: A not so atypical microdeletion syndrome?
β Scribed by Daniela Q.C.M. Barge-Schaapveld; Saskia M. Maas; Abeltje Polstra; Lia C. Knegt; Raoul C.M. Hennekam
- Publisher
- John Wiley and Sons
- Year
- 2011
- Tongue
- English
- Weight
- 208 KB
- Volume
- 155
- Category
- Article
- ISSN
- 1552-4825
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