| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5907246 | Gene | 2012 | 4 Pages |
Abstract
⺠The 15q11.2 syndrome presents with reduced penetrance and/or variable expressivity. ⺠15q11.2 deletion carriers could be at risk of affected offspring. ⺠Clinical spectrum ranges from behavioural features to developmental and speech delay.
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Genetics
Authors
Irene Madrigal, Laia RodrÃguez-Revenga, Mar Xunclà , Montserrat Milà ,