EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: Heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis

A.P. South; G.H.S. Ashton; C. Willoughby; I.H. Ellis; O. Bleck; T. Hamada; G. Mannion; V. Wessagowit; T. Hashimoto; R.A.J. Eady; J.A. Mcgrath

doi:10.1046/j.1365-2133.2002.04638.x

EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: Heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis

A.P. South, G.H.S. Ashton, C. Willoughby, I.H. Ellis, O. Bleck, T. Hamada, G. Mannion, V. Wessagowit, T. Hashimoto, R.A.J. Eady, J.A. Mcgrath

Research output: Contribution to journal › Article › peer-review

20 Citations (Scopus)

Original language	English
Pages (from-to)	216-220
Number of pages	5
Journal	British Journal of Dermatology
Volume	146
Issue number	2
DOIs	https://doi.org/10.1046/j.1365-2133.2002.04638.x
Publication status	Published - 2002

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10.1046/j.1365-2133.2002.04638.x

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South, A. P., Ashton, G. H. S., Willoughby, C., Ellis, I. H., Bleck, O., Hamada, T., Mannion, G., Wessagowit, V., Hashimoto, T., Eady, R. A. J., & Mcgrath, J. A. (2002). EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: Heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis. British Journal of Dermatology, 146(2), 216-220. https://doi.org/10.1046/j.1365-2133.2002.04638.x

South, A.P. ; Ashton, G.H.S. ; Willoughby, C. ; Ellis, I.H. ; Bleck, O. ; Hamada, T. ; Mannion, G. ; Wessagowit, V. ; Hashimoto, T. ; Eady, R.A.J. ; Mcgrath, J.A. / EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: Heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis. In: British Journal of Dermatology. 2002 ; Vol. 146, No. 2. pp. 216-220.

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author = "A.P. South and G.H.S. Ashton and C. Willoughby and I.H. Ellis and O. Bleck and T. Hamada and G. Mannion and V. Wessagowit and T. Hashimoto and R.A.J. Eady and J.A. Mcgrath",

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South, AP, Ashton, GHS, Willoughby, C, Ellis, IH, Bleck, O, Hamada, T, Mannion, G, Wessagowit, V, Hashimoto, T, Eady, RAJ & Mcgrath, JA 2002, 'EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: Heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis', British Journal of Dermatology, vol. 146, no. 2, pp. 216-220. https://doi.org/10.1046/j.1365-2133.2002.04638.x

EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: Heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis. / South, A.P.; Ashton, G.H.S.; Willoughby, C.; Ellis, I.H.; Bleck, O.; Hamada, T.; Mannion, G.; Wessagowit, V.; Hashimoto, T.; Eady, R.A.J.; Mcgrath, J.A.

In: British Journal of Dermatology, Vol. 146, No. 2, 2002, p. 216-220.

Research output: Contribution to journal › Article › peer-review

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T1 - EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: Heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis

AU - South, A.P.

AU - Ashton, G.H.S.

AU - Willoughby, C.

AU - Ellis, I.H.

AU - Bleck, O.

AU - Hamada, T.

AU - Mannion, G.

AU - Wessagowit, V.

AU - Hashimoto, T.

AU - Eady, R.A.J.

AU - Mcgrath, J.A.

N1 - Cited By :19 Export Date: 6 September 2018

PY - 2002

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DO - 10.1046/j.1365-2133.2002.04638.x

M3 - Article

VL - 146

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EP - 220

JO - British Journal of Dermatology

JF - British Journal of Dermatology

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