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Apert syndrome results from localized mutations of FGFR2 and is allelic with Crouzon syndrome

✍ Scribed by Wilkie, Andrew O.M.; Slaney, Sarah F.; Oldridge, Michael; Poole, Michael D.; Ashworth, Geraldine J.; Hockley, Anthony D.; Hayward, Richard D.; David, David J.; Pulleyn, Louise J.; Rutland, Paul

Book ID: 109915171
Publisher: Nature Publishing Group
Year: 1995
Tongue: English
Weight: 1003 KB
Volume: 9
Category: Article
ISSN: 1061-4036
DOI: 10.1038/ng0295-165

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