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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Autors principals:	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
Format:	Journal article
Idioma:	English
Publicat:	2007

Clinical dividends from the molecular genetic diagnosis of craniosynostosis. per 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

Publicat 2007

Journal article

Clinical dividends from the molecular genetic diagnosis of craniosynostosis. per 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

Publicat 2006

Journal article

Clinical dividends from the molecular genetic diagnosis of craniosynostosis.

Clinical dividends from the molecular genetic diagnosis of craniosynostosis. per 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. per 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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