Clinical dividends from the molecular genetic diagnosis of craniosynostosis.

A dozen years have passed since the first genetic lesion was identified in a family with craniosynostosis, the premature fusion of the cranial sutures. Subsequently, mutations in the FGFR2, FGFR3, TWIST1, and EFNB1 genes have been shown to account for approximately 25% of craniosynostosis, whilst se...

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Bibliografiska uppgifter
Huvudupphovsmän:	Wilkie, A, Bochukova, E, Hansen, R, Taylor, I, Rannan-Eliya, S, Byren, J, Wall, SA, Ramos, L, Venâncio, M, Hurst, J, O'rourke, A, Williams, L, Seller, A, Lester, T
Materialtyp:	Journal article
Språk:	English
Publicerad:	2007

Clinical dividends from the molecular genetic diagnosis of craniosynostosis. av Wilkie, A, Bochukova, E, Hansen, R, Taylor, I, Rannan-Eliya, S, Byren, J, Wall, SA, Ramos, L, Venâncio, M, Hurst, J, O'rourke, A, Williams, L, Seller, A, Lester, T

Publicerad 2007

Journal article

Clinical dividends from the molecular genetic diagnosis of craniosynostosis. av Wilkie, A, Bochukova, E, Hansen, R, Taylor, I, Rannan-Eliya, S, Byren, J, Wall, SA, Ramos, L, Venâncio, M, Hurst, J, O'Rourke, A, Williams, L, Seller, A, Lester, T

Publicerad 2006

Journal article

Clinical dividends from the molecular genetic diagnosis of craniosynostosis.

Clinical dividends from the molecular genetic diagnosis of craniosynostosis. av Wilkie, A, Bochukova, E, Hansen, R, Taylor, I, Rannan-Eliya, S, Byren, J, Wall, SA, Ramos, L, Venâncio, M, Hurst, J, O'rourke, A, Williams, L, Seller, A, Lester, T

Clinical dividends from the molecular genetic diagnosis of craniosynostosis. av Wilkie, A, Bochukova, E, Hansen, R, Taylor, I, Rannan-Eliya, S, Byren, J, Wall, SA, Ramos, L, Venâncio, M, Hurst, J, O'Rourke, A, Williams, L, Seller, A, Lester, T

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