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3. Connexin 26 gene linked to a dominant deafness. Denoyelle F; Lina-Granade G; Plauchu H; Bruzzone R; Chaïb H; Lévi-Acobas F; Weil D; Petit C Nature; 1998 May; 393(6683):319-20. PubMed ID: 9620796 [No Abstract] [Full Text] [Related]
4. A new era in the genetics of deafness. Steel KP N Engl J Med; 1998 Nov; 339(21):1545-7. PubMed ID: 9819455 [No Abstract] [Full Text] [Related]
5. 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]
6. Relation between choice of partner and high frequency of connexin-26 deafness. Nance WE; Liu XZ; Pandya A Lancet; 2000 Aug; 356(9228):500-1. PubMed ID: 10981905 [TBL] [Abstract][Full Text] [Related]
7. [From gene to disease: deafness and connexin 26]. Hoefsloot LH; Kemperman M; Cremers CW Ned Tijdschr Geneeskd; 2002 Feb; 146(6):259-61. PubMed ID: 11865655 [TBL] [Abstract][Full Text] [Related]
8. Connexin mutations in deafness. White TW; Deans MR; Kelsell DP; Paul DL Nature; 1998 Aug; 394(6694):630-1. PubMed ID: 9716127 [No Abstract] [Full Text] [Related]
9. High prevalence in the Greek population of the 35delG mutation in the connexin 26 gene causing prelingual deafness. Antoniadi T; Rabionet R; Kroupis C; Aperis GA; Economides J; Petmezakis J; Economou-Petersen E; Estivill X; Petersen MB Clin Genet; 1999 May; 55(5):381-2. PubMed ID: 10422812 [No Abstract] [Full Text] [Related]
15. Multiplex detection of common mutations in the Connexin-26 gene. Baris I; Köksal V Genet Test; 2003; 7(1):63-5. PubMed ID: 12820705 [TBL] [Abstract][Full Text] [Related]
16. Molecular mechanism of a frequent genetic form of deafness. Michel V; Hardelin JP; Petit C N Engl J Med; 2003 Aug; 349(7):716-7. PubMed ID: 12917317 [No Abstract] [Full Text] [Related]
17. Auditory function and the M34T allele of connexin 26. Griffith AJ; Friedman TB Arch Otolaryngol Head Neck Surg; 2002 Jan; 128(1):94. PubMed ID: 11784272 [No Abstract] [Full Text] [Related]
18. Connexin mutations and hearing loss. Scott DA; Kraft ML; Stone EM; Sheffield VC; Smith RJ Nature; 1998 Jan; 391(6662):32. PubMed ID: 9422505 [No Abstract] [Full Text] [Related]
19. DFNA3. Denoyelle F; Weil D; Levilliers J; Petit C Adv Otorhinolaryngol; 2000; 56():78-83. PubMed ID: 10868217 [No Abstract] [Full Text] [Related]