RHBDF2 Mutations Are Associated with Tylosis, a Familial Esophageal Cancer Syndrome von Blaydon, Diana C., Etheridge, Sarah L., Risk, Janet M., Hennies, Hans-Christian, Gay, Laura J., Carroll, Rebecca, Plagnol, Vincent, McRonald, Fiona E., Stevens, Howard P., Spurr, Nigel K., Bishop, D. Timothy, Ellis, Anthony, Jankowski, Janusz, Field, John K., Leigh, Irene M., South, Andrew P., Kelsell, David P.

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Reflectance confocal microscopy to diagnose malignant melanoma and lentigo maligna in the UK: a single-centre prospective observational trial von Stevens, Howard P, Pellacani, Giovanni, Angus, Colin, El-Jabbour, Joseph N

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Reflectance confocal microscopy in diagnosing basal cell carcinoma in the UK: a prospective observational single-centre trial von Stevens, Howard P, Pampena, Riccardo, Farnetani, Francesca, Pellacani, Giovanni, Angus, Colin, El-Jabbour, Joseph N

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Recessive mutation in desmoplakin disrupts desmoplakin-intermediate filament interactions and causes dilated cardiomyopathy, woolly hair and keratoderma von NORGETT, Elizabeth E, HATSELL, Sarah J, CARVAJAL-HUERTA, Luis, CABEZAS, Juan-Carlos Ruiz, COMMON, John, PURKIS, Patricia E, WHITTOCK, Neil, LEIGH, Irene M, STEVENS, Howard P, KELSELL, David P

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The use of Reflectance Confocal Microscopy to diagnose Basal Cell Carcinoma in the United Kingdom: A Prospective Observational Trial at a Single Centre von Stevens, Howard P, Pampena, Riccardo, Farnetani, Francesca, Pellicani, Giovanni, Angus, Colin, El-Jabbour, Joseph N

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Mal de Meleda (MDM) caused by mutations in the gene for SLURP-1 in patients from Germany, Turkey, Palestine, and the United Arab Emirates von ECKL, Katja Martina, STEVENS, Howard P, REIS, André, HENNIES, Hans Christian, LESTRINGANT, Gilles G, WESTENBERGER-TREUMANN, Margaretha, TRAUPE, Heiko, HINZ, Britta, FROSSARD, Philippe M, STADLER, Rudolf, LEIGH, Irene M, NÜRNBERG, Peter

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Mutations in the hair cortex keratin hHb6 cause the inherited hair disease monilethrix von Winter, Hermelita, Rogers, Mike A., Langbein, Lutz, Stevens, Howard P., Leigh, Irene M., Labrèze, Christine, Roul, Sylvie, Taieb, Alain, Krieg, Thomas, Schweizer, Jürgen

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Spectrum of dominant mutations in the desmosomal cadherin desmoglein 1, causing the skin disease striate palmoplantar keratoderma von Hunt, D M, Rickman, L, Whittock, N V, Eady, R A, Simrak, D, Dopping-Hepenstal, P J, Stevens, H P, Armstrong, D K, Hennies, H C, Küster, W, Hughes, A E, Arnemann, J, Leigh, I M, McGrath, J A, Kelsell, D P, Buxton, R S

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Characterization of Paraneoplastic Pemphigus Autoantigens by Immunoblot Analysis von Hashimoto, Takashi, Amagai, Masayuki, Watanabe, Kyoko, Chorzelski, Tadeusz P, Bhogal, Balbir S, Black, Martin M, Stevens, Howard P, Boorsma, Dick M, Korman, Neil J, Gamou, Shinobu, Shimizu, Nobuyoshi, Nishikawa, Takeji

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Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family von Kelsell, D P, Wilgoss, A L, Richard, G, Stevens, H P, Munro, C S, Leigh, I M

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A new mutation in the type II hair cortex keratin hHb1 involved in the inherited hair disorder monilethrix von WINTER, H, ROGERS, M. A, GEBHARDT, M, WOLLINA, U, BOXALL, L, CHITAYAT, D, BABUL-HIRJI, R, STEVENS, H. P, ZLOTOGORSKI, A, SCHWEIZER, J

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An unusual presentation of a common disease von Palamaras, Ioulios, Kench, Peter, Thomson, Penelope, Al-Dulaimi, Abdal Hameed, Stevens, Howard P, Robles, Wanda

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The Gene for Hypotrichosis of Marie Unna Maps between D8S258 and D8S298: Exclusion of the hr Gene by cDNA and Genomic Sequencing von van Steensel, Maurice, Smith, Frances J.D., Steijlen, Peter M., Kluijt, Irma, Stevens, Howard P., Messenger, Andrew, Kremer, Hannie, Dunnill, M. Giles S., Kennedy, Cameron, Munro, Colin S., Doherty, Valerie R., McGrath, John A., Covello, Seana P., Coleman, Carrie M., Uitto, Jouni, McLean, W. H. Irwin

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Working toward a model of demonstrated value in predicting and developing leadership success von Killian, James H., Miller, Corey E., Holmes, Christopher W., Stevens, Howard P.

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N-Terminal Deletion in a Desmosomal Cadherin Causes the Autosomal Dominant Skin Disease Striate Palmoplantar Keratoderma von Rickman, Lisa, Šimrak, Danijela, Stevens, Howard P., Hunt, Debbie M., King, Ian A., Bryant, Stephen P., Eady, Robin A.J., Leigh, Irene M., Arnemann, Joachim, Magee, Anthony I., Kelsell, David P., Buxton, Roger S.

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A Gene for an Autosomal Dominant Scleroatrophic Syndrome Predisposing to Skin Cancer (Huriez Syndrome) Maps to Chromosome 4q23 von Lee, Young-Ae, Stevens, Howard P., Delaporte, Emmanuel, Wahn, Ulrich, Reis, André

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The palmoplantar keratodermas: much more than palms and soles von Kelsell, David P., Stevens, Howard P.

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Connexin mutations associated with palmoplantar keratoderma and profound deafness in a single family von Kelsell, DP, Wilgoss, AL, Richard, G, Stevens, HP, Munro, CS, Leigh, IM

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Localisation of a gene for Papillon-Lefèvre syndrome to chromosome 11q14-q21 by homozygosity mapping von LAASS, M. W, HENNIES, H. C, PREIS, S, STEVENS, H. P, JUNG, M, LEIGH, I. M, WIENKER, T. F, REIS, A

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Close Mapping of the Focal Non-Epidermolytic Palmoplantar Keratoderma (PPK) Locus Associated with Oesophageal Cancer (TOC) von Kelsell, David P., Risk, Janet M., Leigh, Irene M., Stevens, Howard P., Ellis, Anthony, Hennies, Hans C., Reis, André, Weissenbach, Jean, Timothy Bishop, D., Spurr, Nigel K., Field, John K.

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