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Molecular Medicine Today|April 28, 1999
The palmoplantar keratodermas: much more than palms and solesD P Kelsell, H P StevensHuman Molecular Genetics|June 1, 1996
Close mapping of the focal non-epidermolytic palmoplantar keratoderma (PPK) locus associated with oesophageal cancer (TOC)D P Kelsell, J M Risk, I M Leigh, et al.European Journal of Human Genetics : EJHG|April 11, 2000
Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single familyD P Kelsell, A L Wilgoss, G Richard, et al.Experimental Dermatology|October 28, 1999
Fine genetic mapping of diffuse non-epidermolytic palmoplantar keratoderma to chromosome 12q11-q13: exclusion of the mapped type II keratinsD P Kelsell, H P Stevens, P E Purkis, et al.European Journal of Human Genetics : EJHG|July 11, 2000
Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single familyD P Kelsell, A L Wilgoss, G Richard, et al.The British Journal of Dermatology|April 1, 1996
Punctate palmoplantar keratoderma and malignancy in a four-generation familyH P Stevens, D P Kelsell, I M Leigh, et al.The British Journal of Dermatology|June 20, 2002
Diagnosis and confirmation of epidermolytic palmoplantar keratoderma by the identification of mutations in keratin 9 using denaturing high-performance liquid chromatographyE L Rugg, J E A Common, A Wilgoss, et al.Human Molecular Genetics|June 1, 1995
Genetic linkage studies in non-epidermolytic palmoplantar keratoderma: evidence for heterogeneityD P Kelsell, H P Stevens, R Ratnavel, et al.The Journal of Investigative Dermatology|April 1, 1996
Linkage of monilethrix to the trichocyte and epithelial keratin gene cluster on 12q11-q13H P Stevens, D P Kelsell, S P Bryant, et al.Nature|May 1, 1997
Connexin 26 mutations in hereditary non-syndromic sensorineural deafnessD P Kelsell, J Dunlop, H P Stevens, et al.Pageof 13