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6. Novel mutations in the connexin 26 gene (GJB2) that cause autosomal recessive (DFNB1) hearing loss. Kelley PM; Harris DJ; Comer BC; Askew JW; Fowler T; Smith SD; Kimberling WJ Am J Hum Genet; 1998 Apr; 62(4):792-9. PubMed ID: 9529365 [TBL] [Abstract][Full Text] [Related]
7. 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]
8. A missense mutation in connexin26, D66H, causes mutilating keratoderma with sensorineural deafness (Vohwinkel's syndrome) in three unrelated families. Maestrini E; Korge BP; Ocaña-Sierra J; Calzolari E; Cambiaghi S; Scudder PM; Hovnanian A; Monaco AP; Munro CS Hum Mol Genet; 1999 Jul; 8(7):1237-43. PubMed ID: 10369869 [TBL] [Abstract][Full Text] [Related]
9. Prenatal diagnosis of prelingual deafness: carrier testing and prenatal diagnosis of the common GJB2 35delG mutation. Antoniadi T; Pampanos A; Petersen MB Prenat Diagn; 2001 Jan; 21(1):10-3. PubMed ID: 11180233 [TBL] [Abstract][Full Text] [Related]
10. High frequency of the deafness-associated 167delT mutation in the connexin 26 (GJB2) gene in Israeli Ashkenazim. Sobe T; Erlich P; Berry A; Korostichevsky M; Vreugde S; Avraham KB; Bonné-Tamir B; Shohat M Am J Med Genet; 1999 Oct; 86(5):499-500. PubMed ID: 10508996 [No Abstract] [Full Text] [Related]
11. Genetics of congenital deafness in the Palestinian population: multiple connexin 26 alleles with shared origins in the Middle East. Shahin H; Walsh T; Sobe T; Lynch E; King MC; Avraham KB; Kanaan M Hum Genet; 2002 Mar; 110(3):284-9. PubMed ID: 11935342 [TBL] [Abstract][Full Text] [Related]
12. Two different connexin 26 mutations in an inbred kindred segregating non-syndromic recessive deafness: implications for genetic studies in isolated populations. Carrasquillo MM; Zlotogora J; Barges S; Chakravarti A Hum Mol Genet; 1997 Nov; 6(12):2163-72. PubMed ID: 9328482 [TBL] [Abstract][Full Text] [Related]
13. Rapid detection of the 35delG mutation in the GJB2 gene in childhood deafness. Tessa A; Patrono C; Santorelli FM; Giannotti A; Digilio MC; Pacifico C; Presuttari F; Tieri L J Med Screen; 2000; 7(3):167. PubMed ID: 11126168 [No Abstract] [Full Text] [Related]
14. Assignment of connexin 26 (GJB2) and 46 (GJA3) genes to human chromosome 13q11-->q12 and mouse chromosome 14D1-E1 by in situ hybridization. Mignon C; Fromaget C; Mattei MG; Gros D; Yamasaki H; Mesnil M Cytogenet Cell Genet; 1996; 72(2-3):185-6. PubMed ID: 8978770 [No Abstract] [Full Text] [Related]
16. W44C mutation in the connexin 26 gene associated with dominant non-syndromic deafness. Tekin M; Arnos KS; Xia XJ; Oelrich MK; Liu XZ; Nance WE; Pandya A Clin Genet; 2001 Apr; 59(4):269-73. PubMed ID: 11298683 [TBL] [Abstract][Full Text] [Related]
17. Motors, channels and the sounds of silence. Avraham KB Nat Med; 1997 Jun; 3(6):608-9. PubMed ID: 9176483 [No Abstract] [Full Text] [Related]
18. Maternal origin of a de novo mutation of the connexin 26 gene resulting in recessive nonsyndromic deafness. Shalev SA; Hujirat Y Am J Med Genet A; 2004 Feb; 124A(4):411-2. PubMed ID: 14735592 [No Abstract] [Full Text] [Related]
19. A Moroccan family with autosomal recessive sensorineural hearing loss caused by a mutation in the gap junction protein gene connexin 26 (GJB2). Lench NJ; Markham AF; Mueller RF; Kelsell DP; Smith RJ; Willems PJ; Schatteman I; Capon H; Van De Heyning PJ; Van Camp G J Med Genet; 1998 Feb; 35(2):151-2. PubMed ID: 9507396 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]