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22. Keratitis-ichthyosis-deafness syndrome: Phenotypic heterogeneity and treatment perspective of patients with p.Asp50Asn GJB2 mutation. Asgari T; Naji M; Mansouri P; Mahmoudi H; Zabihi M; Youssefian L; Mahdavi M; Naraghi ZS; Zeinali S; Vahidnezhad H; Uitto J Dermatol Ther; 2020 Nov; 33(6):e14493. PubMed ID: 33136289 [TBL] [Abstract][Full Text] [Related]
23. Keratitis, ichthyosis, and deafness (KID) syndrome in half sibs. Koné-Paut I; Hesse S; Palix C; Rey R; Rémédiani K; Garnier JM; Berbis P Pediatr Dermatol; 1998; 15(3):219-21. PubMed ID: 9655320 [TBL] [Abstract][Full Text] [Related]
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33. Ocular Surface Stem Cell Transplantation for Treatment of Keratitis-Ichthyosis-Deafness Syndrome. Cheung AY; Patel S; Kurji KH; Sarnicola E; Eslani M; Govil A; Holland EJ Cornea; 2019 Jan; 38(1):123-126. PubMed ID: 30371567 [TBL] [Abstract][Full Text] [Related]
34. KID Syndrome: report of a Scandinavian patient with connexin-26 gene mutation. Bygum A; Betz RC; Kragballe K; Steiniche T; Peeters N; Wuyts W; Nöthen MM Acta Derm Venereol; 2005; 85(2):152-5. PubMed ID: 15823911 [TBL] [Abstract][Full Text] [Related]
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40. The keratitis, ichthyosis, and deafness (KID) syndrome. Skinner BA; Greist MC; Norins AL Arch Dermatol; 1981 May; 117(5):285-9. PubMed ID: 7224657 [TBL] [Abstract][Full Text] [Related] [Previous] [Next] [New Search]