FGFR2 mutation in a patient without typical features of Pfeiffer syndrome – The emerging role of combined NGS and phenotype based strategies
Author:
Publisher
Elsevier BV
Subject
Genetics (clinical),Genetics,General Medicine
Reference20 articles.
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2. CHARMM: the biomolecular simulation program;Brooks;J. Comput. Chem.,2009
3. FGFR1 and FGFR2 mutations in Pfeiffer syndrome;Chokdeemboon;J. craniofacial Surg.,2013
4. Pfeiffer syndrome update, clinical subtypes, and guidelines for differential diagnosis;Cohen;Am. J. Med. Genet.,1993
5. Of worms and men: an evolutionary perspective on the fibroblast growth factor (FGF) and FGF receptor families;Coulier;J. Mol. Evol.,1997
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