## 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 ✦
Further characterization of microdeletion syndrome involving 2p15-p16.1
✍ Scribed by Têmis Maria Félix; Aline Lourenço Petrin; Maria Teresa Vieira Sanseverino; Jeffrey C. Murray
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 156 KB
- Volume
- 152A
- Category
- Article
- ISSN
- 1552-4825
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