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

Colin Willoughby

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

Colin Willoughby

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

Original language	English
Pages (from-to)	216-220
Number of pages	5
Journal	British Journal of Dermatology
Volume	146(2)
Issue number	2
Publication status	Published - 2002

ASJC Scopus subject areas

Dermatology

Cite this

@article{cf012c4509c6402dbbf5f4bc52110a0a,

title = "EEC (Ectrodactyly, Ectodermal dysplasia, Clefting) syndrome: heterozygous mutation in the p63 gene (R279H) and DNA-based prenatal diagnosis.",

author = "Colin Willoughby",

year = "2002",

language = "English",

volume = "146(2)",

pages = "216--220",

journal = "British Journal of Dermatology",

issn = "1365-2133",

publisher = "Oxford University Press",

number = "2",

}

TY - JOUR

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

AU - Willoughby, Colin

PY - 2002

Y1 - 2002

UR - http://www.scopus.com/inward/record.url?scp=0036207517&partnerID=8YFLogxK

M3 - Article

C2 - 11903230

SN - 1365-2133

VL - 146(2)

SP - 216

EP - 220

JO - British Journal of Dermatology

JF - British Journal of Dermatology

IS - 2

ER -

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

ASJC Scopus subject areas

Other files and links

Cite this