Letter to the Editor
Journal of Investigative Dermatology (2002) 119, 1202–1203; 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
Takahiro Hamada, Ien Chan, Colin E Willoughby*, David R Goudie† and John A McGrath
- Department of Cell and Molecular Pathology, St John's Institute of Dermatology, The Guy's, King's College and St Thomas' Hospitals' Medical School, St Thomas' Hospital, London, U.K.
- *Experimental Ophthalmology Unit, Department of Medicine, University of Liverpool, Liverpool, U.K.
- †Department of Medicine, Clinical Genetics, Human Genetics Unit, Ninewells Hospital and Medical School, Dundee, U.K.
Correspondence: John McGrath, Department of Cell and Molecular Pathology, St John's Institute of Dermatology, The Guy's, King's College and St Thomas' Hospitals' Medical School, St Thomas' Hospital, London, U.K. email: john.mcgrath@rcl.ac.uk
Received 3 April 2002; Revised 13 June 2002; Accepted 18 July 2002.
