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.
- PubMed ID
- 16061565 [ View in PubMed]
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