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Neurotological and neuroanatomical changes in the connexin-26-related HID/KID syndromeTODT, I; HENNIES, H. C; KÜSTER, W et al.Audiology & neuro-otology. 2006, Vol 11, Num 4, pp 242-248, issn 1420-3030, 7 p.Article

A novel connexin 26 gene mutation associated with features of the keratitis-ichthyosis-deafness syndrome and the follicular occlusion triadMONTGOMERY, Jay R; WHITE, Thomas W; MARTIN, Bryan L et al.Journal of the American Academy of Dermatology. 2004, Vol 51, Num 3, pp 377-382, issn 0190-9622, 6 p.Article

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Keratitis-ichthyosis-deafness syndrome and carotenaemiaAHMADI, S; MCKENNA, K.Clinical and experimental dermatology (Print). 2003, Vol 28, Num 4, pp 394-396, issn 0307-6938, 3 p.Article

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What syndrome is this?LENANE, Patsy; CAMMISULI, Sam; CHITAYAT, David et al.Pediatric dermatology. 2006, Vol 23, Num 1, pp 81-83, issn 0736-8046, 3 p.Article

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KID versus KED : What's in a nameWILLIAMS, M. L; MCCALMONT, T. H.Pediatric dermatology. 1996, Vol 13, Num 2, pp 154-157, issn 0736-8046Article

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Differential susceptibility of Cx26 mutations associated with epidermal dysplasias to peptidoglycan derived from Staphylococcus aureus and Staphylococcus epidermidisDONNELLY, Steven; ENGLISH, Grant; DE ZWART-STORM, Eugene A et al.Experimental dermatology. 2012, Vol 21, Num 8, pp 592-598, issn 0906-6705, 7 p.Article

Genetic heterogeneity of KID syndrome: Identification of a Cx30 gene (GJB6) mutation in a patient with KID syndrome and congenital atrichiaJAN, Amy Y; AMIN, Shivan; RATAJCZAK, Paulina et al.Journal of investigative dermatology. 2004, Vol 122, Num 5, pp 1108-1113, issn 0022-202X, 6 p.Article

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