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Phenotypic and molecular characterization of a novel DCX deletion and a review of the literature

✍ Scribed by A Chou; C Boerkoel; C Du Souich; R Rupps


Book ID
110888819
Publisher
John Wiley and Sons
Year
2009
Tongue
English
Weight
493 KB
Volume
76
Category
Article
ISSN
0009-9163

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Clinical and molecular characterization
✍ Ulrika Wester; Marie-Louise Bondeson; Christina Edeby; Göran Annerén 📂 Article 📅 2006 🏛 John Wiley and Sons 🌐 English ⚖ 112 KB 👁 3 views

## Abstract The deletion 18p syndrome is one of the most common chromosome abnormalities. The medical problems are mental and postnatal growth retardation, and sometimes malformations of the heart and brain. The individuals have some typical features, which might be easy to overlook and which are: