Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain.

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McGillivray G, Savarirayan R, Cox TC, Stojkoski C, McNeil R, Bankier A, Bateman JF, Roscioli T, Gardner RJ, Lamande SR

Familial scaphocephaly syndrome caused by a novel mutation in the FGFR2 tyrosine kinase domain.

J Med Genet. 2005 Aug;42(8):656-62.

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16061565 [ View in PubMed
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Polypeptides
NameUniProt ID
Fibroblast growth factor receptor 2P21802Details