Fibroblast Growth Factor Receptor-2 Mutations in Craniosynostosisa
Author:
Publisher
Wiley
Subject
History and Philosophy of Science,General Biochemistry, Genetics and Molecular Biology,General Neuroscience
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1749-6632.1996.tb56255.x/fullpdf
Reference29 articles.
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2. Control of BEK and K-SAM splice sites in alternative splicing of the fibroblast growth factor receptor 2 pre-mRNA;Gilbert;Mol. Cell Biol.,1993
3. Fatal familial insomnia and familial Creutzfeld-Jakob disease: Disease phenotype determined by a DNA polymorphism;Goldfarb;Science,1992
4. Crouzon syndrome: Mutations in two spiceoforms of FGFR2 and a common point mutation shared with Jackson-Weiss syndrome;Gorry;Hum. Mol. Genet.,1995
5. Related fibroblast growth factor receptor genes exist in the human genome;Houssaint;Proc. Natl. Acad. Sci. U.S.A.,1990
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