D.P. Kelsell
Centre for Cutaneous Research
St Bartholomew's and The Royal London School of Medicine and Dentistry
Queen Mary and Westfield College
UK
Name/email consistency: high
- Connexin mutations in skin disease and hearing loss. Kelsell, D.P., Di, W.L., Houseman, M.J. Am. J. Hum. Genet. (2001)
- Spotting prostate cancer. Neill, G.W., Kelsell, D.P. Trends. Mol. Med (2001)
- Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family. Kelsell, D.P., Wilgoss, A.L., Richard, G., Stevens, H.P., Munro, C.S., Leigh, I.M. Eur. J. Hum. Genet. (2000)
- Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family. Kelsell, D.P., Wilgoss, A.L., Richard, G., Stevens, H.P., Munro, C.S., Leigh, I.M. Eur. J. Hum. Genet. (2000)
- The palmoplantar keratodermas: much more than palms and soles. Kelsell, D.P., Stevens, H.P. Mol. Med. Today (1999)
- Fine genetic mapping of diffuse non-epidermolytic palmoplantar keratoderma to chromosome 12q11-q13: exclusion of the mapped type II keratins. Kelsell, D.P., Stevens, H.P., Purkis, P.E., Talas, U., Rustin, M.H., Leigh, I.M. Exp. Dermatol. (1999)
