Common mutations in Arg304 of the p63 gene in Ectrodactyly, Ectodermal Dysplasia, Clefting syndrome: lack of genotype-phenotype correlation and implications for mutation detection strategies.

T. Hamada; I. Chan; Colin Willoughby; D.R. Goudie; J.A. McGrath

Common mutations in Arg304 of the p63 gene in Ectrodactyly, Ectodermal Dysplasia, Clefting syndrome: lack of genotype-phenotype correlation and implications for mutation detection strategies.

T. Hamada, I. Chan, Colin Willoughby, D.R. Goudie, J.A. McGrath

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

Original language	English
Pages (from-to)	1202-1203
Number of pages	2
Journal	Journal of investigative dermatology
Volume	119(5)
Issue number	5
Publication status	Published - Nov 2002

ASJC Scopus subject areas

Dermatology

Cite this

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title = "Common mutations in Arg304 of the p63 gene in Ectrodactyly, Ectodermal Dysplasia, Clefting syndrome: lack of genotype-phenotype correlation and implications for mutation detection strategies.",

author = "T. Hamada and I. Chan and Colin Willoughby and D.R. Goudie and J.A. McGrath",

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Common mutations in Arg304 of the p63 gene in Ectrodactyly, Ectodermal Dysplasia, Clefting syndrome: lack of genotype-phenotype correlation and implications for mutation detection strategies. / Hamada, T.; Chan, I.; Willoughby, Colin et al.
In: Journal of investigative dermatology, Vol. 119(5), No. 5, 11.2002, p. 1202-1203.

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

TY - JOUR

T1 - Common mutations in Arg304 of the p63 gene in Ectrodactyly, Ectodermal Dysplasia, Clefting syndrome: lack of genotype-phenotype correlation and implications for mutation detection strategies.

AU - Hamada, T.

AU - Chan, I.

AU - Willoughby, Colin

AU - Goudie, D.R.

AU - McGrath, J.A.

PY - 2002/11

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M3 - Article

SN - 1523-1747

VL - 119(5)

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JO - Journal of investigative dermatology

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Common mutations in Arg304 of the p63 gene in Ectrodactyly, Ectodermal Dysplasia, Clefting syndrome: lack of genotype-phenotype correlation and implications for mutation detection strategies.

ASJC Scopus subject areas

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