Craniofacial dyssynostosis with cryptorchidism and normal stature
Author:
Publisher
Wiley
Subject
Genetics (clinical)
Reference4 articles.
1. (1994): ?Mendelian Inheritance in Man.? 11th ed. Baltimore: Johns Hopkins University Press.
2. A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome
3. Studies of malformation syndromes of man XXXIX: A craniosynostosis-craniofacial dysostosis syndrome with mental retardation and other malformations: ?Craniofacial dyssynostosis?
4. Identical mutations in the FGFR2 gene cause both Pfeiffer and Crouzon syndrome phenotypes
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