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6. A novel connexin 26 mutation in a patient diagnosed with keratitis-ichthyosis-deafness syndrome. van Steensel MA; van Geel M; Nahuys M; Smitt JH; Steijlen PM J Invest Dermatol; 2002 Apr; 118(4):724-7. PubMed ID: 11918723 [TBL] [Abstract][Full Text] [Related]
9. A report of GJB2 (N14K) Connexin 26 mutation in two patients--a new subtype of KID syndrome? Lazic T; Horii KA; Richard G; Wasserman DI; Antaya RJ Pediatr Dermatol; 2008; 25(5):535-40. PubMed ID: 18950394 [TBL] [Abstract][Full Text] [Related]
10. Severe form of keratitis-ichthyosis-deafness (KID) syndrome associated with septic complications. Haruna K; Suga Y; Oizumi A; Mizuno Y; Endo H; Shimizu T; Hasegawa T; Ikeda S J Dermatol; 2010 Jul; 37(7):680-2. PubMed ID: 20629838 [No Abstract] [Full Text] [Related]
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13. Treatment of keratitis-ichthyosis- deafness (KID) syndrome in children: a case report and review of the literature. Patel V; Sun G; Dickman M; Khuu P; Teng JM Dermatol Ther; 2015; 28(2):89-93. PubMed ID: 25546246 [TBL] [Abstract][Full Text] [Related]
14. Germline mosaicism in keratitis-ichthyosis-deafness syndrome: pre-natal diagnosis in a familial lethal form. Sbidian E; Feldmann D; Bengoa J; Fraitag S; Abadie V; de Prost Y; Bodemer C; Hadj-Rabia S Clin Genet; 2010 Jun; 77(6):587-92. PubMed ID: 20412116 [TBL] [Abstract][Full Text] [Related]
16. A novel dominant and a de novo mutation in the GJB2 gene (connexin-26) cause keratitis-ichthyosis-deafness syndrome: implication for cochlear implantation. Arndt S; Aschendorff A; Schild C; Beck R; Maier W; Laszig R; Birkenhäger R Otol Neurotol; 2010 Feb; 31(2):210-5. PubMed ID: 20101161 [TBL] [Abstract][Full Text] [Related]