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


Autoria(s): Willoughby, Colin
Data(s)

2002

Identificador

http://pure.qub.ac.uk/portal/en/publications/eec-ectrodactyly-ectodermal-dysplasia-clefting-syndrome-heterozygous-mutation-in-the-p63-gene-r279h-and-dnabased-prenatal-diagnosis(cf012c45-09c6-402d-bbf5-f4bc52110a0a).html

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

Idioma(s)

eng

Direitos

info:eu-repo/semantics/restrictedAccess

Fonte

Willoughby , C 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(2) , no. 2 , pp. 216-220 .

Palavras-Chave #/dk/atira/pure/subjectarea/asjc/2700/2708 #Dermatology
Tipo

article