A syndromic form of Pierre Robin sequence is caused by 5q23 deletions encompassing FBN2 and PHAX
- 1 October 2014
- journal article
- research article
- Published by Elsevier in European Journal of Medical Genetics
- Vol. 57 (10) , 587-595
Abstract
No abstract availableKeywords
Funding Information
- MRC Human Genetics Unit
- ERare CRANIRARE
- ANR IHU
- Centre de Référence Maladie Rare Pierre Robin
- Wellcome Trust
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