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

    19 Citations (Scopus)
    LanguageEnglish
    Pages216-220
    Number of pages5
    JournalBritish Journal of Dermatology
    Volume146
    Issue number2
    DOIs
    Publication statusPublished - 2002

    Cite this

    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",
    note = "Cited By :19 Export Date: 6 September 2018",
    year = "2002",
    doi = "10.1046/j.1365-2133.2002.04638.x",
    language = "English",
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    pages = "216--220",
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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

    TY - JOUR

    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

    Y1 - 2002

    U2 - 10.1046/j.1365-2133.2002.04638.x

    DO - 10.1046/j.1365-2133.2002.04638.x

    M3 - Article

    VL - 146

    SP - 216

    EP - 220

    JO - British Journal of Dermatology

    T2 - British Journal of Dermatology

    JF - British Journal of Dermatology

    SN - 0007-0963

    IS - 2

    ER -

    South AP, Ashton GHS, Willoughby C, Ellis IH, Bleck O, Hamada T et al. EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: Heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis. British Journal of Dermatology. 2002;146(2):216-220. https://doi.org/10.1046/j.1365-2133.2002.04638.x

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