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 [1]

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

doi:10.1046/j.1523-1747.2002.19526.x

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 [1]

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

Research output: Contribution to journal › Article

Original language	English
Pages (from-to)	1202-1203
Number of pages	2
Journal	Journal of Investigative Dermatology
Volume	119
Issue number	5
DOIs	https://doi.org/10.1046/j.1523-1747.2002.19526.x
Publication status	Published - 2002

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Hamada, T., Chan, I., Willoughby, C. E., Goudie, D. R., & McGrath, J. A. (2002). 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 [1]. Journal of Investigative Dermatology, 119(5), 1202-1203. https://doi.org/10.1046/j.1523-1747.2002.19526.x

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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 [1]",

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

note = "Cited By :9 Export Date: 6 September 2018",

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Hamada, T, Chan, I, Willoughby, CE, Goudie, DR & McGrath, JA 2002, '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 [1]', Journal of Investigative Dermatology, vol. 119, no. 5, pp. 1202-1203. https://doi.org/10.1046/j.1523-1747.2002.19526.x

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 [1]. / Hamada, T.; Chan, I.; Willoughby, C.E.; Goudie, D.R.; McGrath, J.A.

In: Journal of Investigative Dermatology, Vol. 119, No. 5, 2002, p. 1202-1203.

Research output: Contribution to journal › Article

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 [1]

AU - Hamada, T.

AU - Chan, I.

AU - Willoughby, C.E.

AU - Goudie, D.R.

AU - McGrath, J.A.

N1 - Cited By :9 Export Date: 6 September 2018

PY - 2002

Y1 - 2002

U2 - 10.1046/j.1523-1747.2002.19526.x

DO - 10.1046/j.1523-1747.2002.19526.x

M3 - Article

VL - 119

SP - 1202

EP - 1203

JO - Journal of Investigative Dermatology

JF - Journal of Investigative Dermatology

SN - 0022-202X

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ER -