| 1 | CRS7A, CRS7C, FGFR1, FGFR2
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| FGFR1 and FGFR2 Mutations in Pfeiffer Syndrome.
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| Chokdeemboon C, Mahatumarat C, Rojvachiranonda N, Tongkobpetch S, Suphapeetiporn K, Shotelersuk V.
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| J Craniofac Surg 24(1):150-2. doi: 10.1097/SCS.0b013e3182646454.
2013
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| 2 | CRS7C, FGFR2
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| 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.
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| J Med Genet 42(8):656-62. No abstract available. 2005
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