A case of erythrokeratoderma variabilis without mutations in connexin 31
Ishida‐Yamamoto, A., Kelsell, D., Common, J., Houseman, M.J., Hashimoto, M., Shibaki, H., Asano, K., Takahashi, H., Hashimoto, Y., Senshu, T., Leigh, I.M., Iizuka, H.
Published in British journal of dermatology (1951) (01.12.2000)
Published in British journal of dermatology (1951) (01.12.2000)
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Prelingual Deafness: High Prevalence of a 30delG Mutation in the Connexin 26 Gene
Denoyelle, Françoise, Weil, Dominique, Maw, Marion A., Wilcox, Stephen A., Lench, Nicholas J., Allen-Powell, Denise R., Osborn, Amelia H., Dahl, Hans-Henrik M., Middleton, Anna, Houseman, Mark J., Dodé, Catherine, Marlin, Sandrine, Boulila-ElGaïed, Amel, Grati, Mohammed, Ayadi, Hammadi, BenArab, Saïda, Bitoun, Pierre, Lina-Granade, Geneviève, Godet, Jacqueline, Mustapha, Mirna, Loiselet, Jacques, El-Zir, Élie, Aubois, Anne, Joannard, Alain, Levilliers, Jacqueline, Garabédian, Éréa-Noël, Mueller, Robert F., McKinlay Gardner, R. J., Petit, Christine
Published in Human molecular genetics (01.11.1997)
Published in Human molecular genetics (01.11.1997)
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Connexin Mutations in Skin Disease and Hearing Loss
Kelsell, David P., Di, Wei-Li, Houseman, Mark J.
Published in American journal of human genetics (01.03.2001)
Published in American journal of human genetics (01.03.2001)
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Genetic analysis of the connexin-26 M34T variant: identification of genotype M34T/M34T segregating with mild-moderate non-syndromic sensorineural hearing loss
Houseman, Mark J, Ellis, Lucy A, Pagnamenta, Alistair, Di, Wei-Li, Rickard, Sarah, Osborn, Amelia H, Dahl, Hans-Henrik M, Taylor, Graham R, Bitner-Glindzicz, Maria, Reardon, William, Mueller, Robert F, Kelsell, David P
Published in Journal of medical genetics (01.01.2001)
Published in Journal of medical genetics (01.01.2001)
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