Distinct craniofacial-skeletal-dermatological dysplasia in a patient with W290C mutation inFGFR2
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference10 articles.
1. 2001. Craniosynostosis syndromes. In: editors. The metabolic and molecular bases of inherited disease. New York: McGraw-Hill. p 6117-6146.
2. Mutations in the third immunoglobulin domain of the fibroblast growth factor receptor-2 gene in Crouzon syndrome
3. Novel FGFR2 mutations in Crouzon and Jackson-Weiss syndromes show allelic heterogeneity and phenotypic variability
4. Clinical spectrum of fibroblast growth factor receptor mutations
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