Isolated Sagittal Synostosis in a Boy with Craniofrontonasal Dysplasia and a Novel EFNB1 Mutation
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Surgery,Surgery
Reference26 articles.
1. Mutations of the Ephrin-B1 Gene Cause Craniofrontonasal Syndrome
2. Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome
3. A Novel de Novo Mutation Within EFNB1 Gene in a Young Girl with Craniofrontonasal Syndrome
4. Diverse Clinical and Genetic Aspects of Craniofrontonasal Syndrome
5. Clinical and genetic aspects of craniofrontonasal syndrome: Towards resolving a genetic paradox
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