Patients Carrying 9q31.1-q32 Deletion Share Common Features with Cornelia de Lange Syndrome
Background: Cornelia de Lange Syndrome (CdLS) is a rare but severe clinically heterogeneous developmental disorder characterized by facial dysmorphia, growth and cognitive retardation, and abnormalities of limb development. Objectives: To determine the pathogenesis of a patient with CdLS. Methods: W...
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| Asıl Yazarlar: | , , , , , , , , |
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| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Cell Physiol Biochem Press GmbH & Co KG
2015-01-01
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| Seri Bilgileri: | Cellular Physiology and Biochemistry |
| Konular: | |
| Online Erişim: | http://www.karger.com/Article/FullText/369694 |
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