Syndrome de keratitis-ichthyosis-deafness (KID) = Keratitis-ichthyosis-deafness (KID) syndromeMAZEREEUW-HAUTIER, J.Annales de dermatologie et de vénéréologie. 2008, Vol 135, Num 1, pp 80-82, issn 0151-9638, 3 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

Keratitis-Ichthyosis-Deafness Syndrome Lacking Subjective Hearing ImpairmentNEMOTO-HASEBE, Ikue; AKIYAMA, Masashi; YAMADA, Nanako et al.Acta dermato-venereologica. 2008, Vol 88, Num 4, pp 406-408, issn 0001-5555, 3 p.Article

KID syndrome : Report of a scandinavian patient with connexin-26 gene mutationBYGUM, Anette; BETZ, Regina C; KRAGBALLE, Knud et al.Acta dermato-venereologica. 2005, Vol 85, Num 2, pp 152-155, issn 0001-5555, 4 p.Article

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

Possible modifier effects of keratin 17 gene mutation on keratitis―ichthyosis―deafness syndromeNATSUGA, K; SHINKUMA, S; KANDA, M et al.British journal of dermatology (1951). 2012, Vol 166, Num 4, pp 903-905, issn 0007-0963, 3 p.Article

A novel mutation in the connexin 26 gene (GJB2) in a child with clinical and histological features of keratitis―ichthyosis―deafness (KID) syndromeKOPPELHUS, U; TRANEBJÆRG, L; ESBERG, G et al.Clinical and experimental dermatology (Print). 2011, Vol 36, Num 2, pp 142-148, issn 0307-6938, 7 p.Article

Keratitis-ichthyosis-deafness (KID) syndrome with squamous cell carcinomaCONRADO, Luciana A; MARQUES, Silvio A; LASTORIA, Joel C et al.International journal of dermatology. 2007, Vol 46, Num 4, pp 403-406, issn 0011-9059, 4 p.Article

A case of keratitis-ichthyosis-deafness (KID) syndromeWATANABE, Daisuke; ZAKO, Mcasahiro; TAMADA, Yasuhiko et al.International journal of dermatology. 2007, Vol 46, Num 4, pp 400-402, issn 0011-9059, 3 p.Article

Cochleosaccular dysplasia associated with a connexin 26 mutation in keratitis-ichthyosis-deafness syndromeGRIFFITH, Andrew J; YANDAN YANG; MERCHANT, Saumil N et al.The Laryngoscope. 2006, Vol 116, Num 8, pp 1404-1408, issn 0023-852X, 5 p.Article

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

Keratitis-Ichthyosis-Deafness Syndrome: Response to Alitretinoin and Review of LiteratureWERCHAU, Siegfried; TOBERER, Ferdinand; ENK, Alexander et al.Archives of dermatology (1960). 2011, Vol 147, Num 8, pp 993-995, issn 0003-987X, 3 p.Article

Porokeratotic Eccrine Duct and Hair Follicle Nevus (PEHFN) Associated with Keratitis-Ichthyosis-Deafness (KID) SyndromeCRISCIONE, Vincent; LACHIEWICZ, Anne; ROBINSON-BOSTOM, Leslie et al.Pediatric dermatology. 2010, Vol 27, Num 5, pp 514-517, issn 0736-8046, 4 p.Article

A rare connexin 26 mutation in a patient with a forme fruste of keratitis-ichthyosis-deafness (KID) syndromeCHING YIN NEOH; HUIJIA CHEN; SEE KET NG et al.International journal of dermatology. 2009, Vol 48, Num 10, pp 1078-1081, issn 0011-9059, 4 p.Article

Two patients with severe corneal disease in KID syndromeSONODA, Shozo; UCHINO, Eisuke; SONODA, Koh-Hei et al.American journal of ophthalmology. 2004, Vol 137, Num 1, pp 181-183, issn 0002-9394, 3 p.Article

KID syndrome : Une cause de pachydermatoglyphie = KID syndrome: a cause of pachydermatoglyphiaBOUDGHENE STAMBOULI, O; BELBACHIR, A.Annales de dermatologie et de vénéréologie. 2003, Vol 130, Num 12, pp 1143-1145, issn 0151-9638, 3 p., CAH1Article

Connexin 26 mutation in keratitis-ichthyosis-deafness (KID) syndrome in mother and daughter with combined conductive and sensorineural hearing lossKELLY, Brent; LOZANO, Annabelle; ALTENBERG, Guillermo et al.International journal of dermatology. 2008, Vol 47, Num 5, pp 443-447, issn 0011-9059, 5 p.Article

A novel N14Y mutation in connexin26 in keratitis- ichthyosis-deafness syndrome : Analyses of altered gap junctional communication and molecular structure of N terminus of mutated connexin26ARITA, Ken; AKIYAMA, Masashi; AIZAWA, Tomoyasu et al.The American journal of pathology. 2006, Vol 169, Num 2, pp 416-423, issn 0002-9440, 8 p.Article

Syndrome Keratitis-Ichtyosis-Deafness (KID): une observation chez un enfant en Afrique subsaharienne = Keratitis-Ichtyosis-Deafness (KID) syndrome: An observation in a child in sub-saharan AfricaBARRUET, K; SAKA, B; KOMBATE, K et al.Annales de dermatologie et de vénéréologie. 2011, Vol 138, Num 5, pp 453-455, issn 0151-9638, 3 p.Article

The connexin26 S17F mouse mutant represents a model for the human hereditary keratitis― ichthyosis―deafness syndromeSCHÜTZ, Melanie; AUTH, Tanja; GEHRT, Anna et al.Human molecular genetics (Print). 2011, Vol 20, Num 1, pp 28-39, issn 0964-6906, 12 p.Article

Trichothiodystrophy-like Hair Abnormalities in a Child with Keratitis Ichthyosis Deafness SyndromeDE RAEVE, L; BONDUELLE, M; DECONINCK, H et al.Pediatric dermatology. 2008, Vol 25, Num 4, pp 466-469, issn 0736-8046, 4 p.Article

Keratitis-ichthyosis-deafness syndrome in association with follicular occlusion triadMAINTZ, Laura; BETZ, Regina C; ALLAM, Jean-Pierre et al.EJD. European journal of dermatology. 2005, Vol 15, Num 5, pp 347-352, issn 1167-1122, 6 p.Article

A Report of GJB2 (N14K) Connexin 26 Mutation in Two Patients : A New Subtype of KID Syndrome?LAZIC, Tamara; HORII, Kimberly A; RICHARD, Gabriele et al.Pediatric dermatology. 2008, Vol 25, Num 5, pp 535-540, issn 0736-8046, 6 p.Article

A familial case of Keratitis-Ichthyosis-Deafness (KID) syndrome with the GJB2 mutation G45EJONARD, Laurence; FELDMANN, Delphine; MARLIN, Sandrine et al.European journal of medical genetics. 2008, Vol 51, Num 1, pp 35-43, issn 1769-7212, 9 p.Article

GJB2 mutations in keratitis-ichthyosis-deafness syndrome including its fatal formJANECKE, Andreas R; HENNIES, Hans Christian; GÜNTHER, Barbara et al.American journal of medical genetics. 2005, Vol 133A, Num 2, pp 128-131, issn 0148-7299, 4 p.Article