Bad bones, absent smell, selfish testes: The pleiotropic consequences of human FGF receptor mutations
Author:
Publisher
Elsevier BV
Subject
General Biochemistry, Genetics and Molecular Biology,Immunology,Immunology and Allergy,Endocrinology, Diabetes and Metabolism
Reference158 articles.
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3. Mutations in the fibroblast growth factor receptor 2 gene cause Crouzon syndrome;Reardon;Nat Genet,1994
4. Jackson–Weiss and Crouzon syndromes are allelic with mutations in fibroblast growth factor receptor 2;Jabs;Nat Genet,1994
5. A common mutation in the fibroblast growth factor receptor 1 gene in Pfeiffer syndrome;Muenke;Nat Genet,1994
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