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22. [Detection with restriction enzyme for mutation 233delC of the connexin26 gene]. Hanamitsu M; Suzuki M; Kitano H; Kitanishi T Nihon Jibiinkoka Gakkai Kaiho; 2002 Jul; 105(7):799-803. PubMed ID: 12174613 [TBL] [Abstract][Full Text] [Related]
23. 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]
34. More on the genetics of prelingual deafness. Majumder PP; Ramesh A; Chinnappan D Am J Hum Genet; 1989 Oct; 45(4):638-40. PubMed ID: 2491021 [No Abstract] [Full Text] [Related]
35. Further comments on the genetics of prelingual deafness. Marazita ML; Nance WE; Arnos KS Am J Hum Genet; 1989 Oct; 45(4):637-8. PubMed ID: 2491020 [No Abstract] [Full Text] [Related]
36. Prelingual deafness: high prevalence of a 30delG mutation in the connexin 26 gene. Denoyelle F; Weil D; Maw MA; Wilcox SA; Lench NJ; Allen-Powell DR; Osborn AH; Dahl HH; Middleton A; Houseman MJ; Dodé C; Marlin S; Boulila-ElGaïed A; Grati M; Ayadi H; BenArab S; Bitoun P; Lina-Granade G; Godet J; Mustapha M; Loiselet J; El-Zir E; Aubois A; Joannard A; Levilliers J; Garabédian EN; Mueller RF; Gardner RJ; Petit C Hum Mol Genet; 1997 Nov; 6(12):2173-7. PubMed ID: 9336442 [TBL] [Abstract][Full Text] [Related]