Apert and Pfeiffer syndromes are hereditary forms of craniosynostosis characterized by midfacial hypoplasia and malformations of the limbs and skull. A serious consequence of midfacial hypoplasia in these syndromes is respiratory compromise due to airway obstruction. In this study, we have evaluated
β¦ LIBER β¦
Brain phenotypes in two FGFR2 mouse models for Apert syndrome
β Scribed by Kristina Aldridge; Cheryl A. Hill; Jordan R. Austin; Christopher Percival; Neus Martinez-Abadias; Thomas Neuberger; Yingli Wang; Ethylin Wang Jabs; Joan T. Richtsmeier
- Publisher
- John Wiley and Sons
- Year
- 2010
- Tongue
- English
- Weight
- 646 KB
- Volume
- 239
- Category
- Article
- ISSN
- 1058-8388
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