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5. Genotypic and phenotypic correlations of DFNB1-related hearing impairment in the Midwestern United States. Lim LH; Bradshaw JK; Guo Y; Pilipenko V; Madden C; Ingala D; Keddache M; Choo DI; Wenstrup R; Greinwald JH Arch Otolaryngol Head Neck Surg; 2003 Aug; 129(8):836-40. PubMed ID: 12925341 [TBL] [Abstract][Full Text] [Related]
6. Temporal bone imaging in GJB2 deafness. Propst EJ; Blaser S; Stockley TL; Harrison RV; Gordon KA; Papsin BC Laryngoscope; 2006 Dec; 116(12):2178-86. PubMed ID: 17146393 [TBL] [Abstract][Full Text] [Related]
7. [The audiological phenotype and the prevalence of GJB2-related sensorineural loss of hearing in the infants suffering acoustic disturbances]. Lalaiants MR; Markova TG; Bakhshinian VV; Bliznets EA; Poliakov AV; Tavartikiladze GA Vestn Otorinolaringol; 2014; (2):37-43. PubMed ID: 24781170 [TBL] [Abstract][Full Text] [Related]
8. Additional clinical manifestations in children with sensorineural hearing loss and biallelic GJB2 mutations: who should be offered GJB2 testing? Kenna MA; Rehm HL; Robson CD; Frangulov A; McCallum J; Yaeger D; Krantz ID Am J Med Genet A; 2007 Jul; 143A(14):1560-6. PubMed ID: 17455295 [TBL] [Abstract][Full Text] [Related]
9. The Yield of Multigene Testing in the Management of Pediatric Unilateral Sensorineural Hearing Loss. Gruber M; Brown C; Mahadevan M; van der Meer G; Neeff M Otol Neurotol; 2016 Sep; 37(8):1066-70. PubMed ID: 27466889 [TBL] [Abstract][Full Text] [Related]
11. GJB2 allele variants and the associated audiologic features identified in Chinese patients with less severe idiopathic hearing loss. Zhang J; Wang Z; Dai W; Zeng Y; Li H Genet Test Mol Biomarkers; 2011 May; 15(5):313-8. PubMed ID: 21366436 [TBL] [Abstract][Full Text] [Related]
12. GJB2 mutations and genotype-phenotype correlation in 335 patients from germany with nonsyndromic sensorineural hearing loss: evidence for additional recessive mutations not detected by current methods. Bartsch O; Vatter A; Zechner U; Kohlschmidt N; Wetzig C; Baumgart A; Nospes S; Haaf T; Keilmann A Audiol Neurootol; 2010; 15(6):375-82. PubMed ID: 20234132 [TBL] [Abstract][Full Text] [Related]
13. GJB2 mutations: Genotypic and phenotypic correlation in a cohort of 690 hearing-impaired patients, toward a new mutation? Leclère JC; Le Gac MS; Le Maréchal C; Ferec C; Marianowski R Int J Pediatr Otorhinolaryngol; 2017 Nov; 102():80-85. PubMed ID: 29106882 [TBL] [Abstract][Full Text] [Related]
14. Phenotype/genotype correlations in a DFNB1 cohort with ethnical diversity. Angeli SI Laryngoscope; 2008 Nov; 118(11):2014-23. PubMed ID: 18758381 [TBL] [Abstract][Full Text] [Related]
16. Phenotypes of two Dutch DFNA3 families with mutations in GJB2. Weegerink NJ; Pennings RJ; Huygen PL; Hoefsloot LH; Cremers CW; Kunst HP Ann Otol Rhinol Laryngol; 2011 Mar; 120(3):191-7. PubMed ID: 21510145 [TBL] [Abstract][Full Text] [Related]
17. Connexin 26 studies in patients with sensorineural hearing loss. Kenna MA; Wu BL; Cotanche DA; Korf BR; Rehm HL Arch Otolaryngol Head Neck Surg; 2001 Sep; 127(9):1037-42. PubMed ID: 11556849 [TBL] [Abstract][Full Text] [Related]
18. The influence of mutations in the SLC26A4 gene on the temporal bone in a population with enlarged vestibular aqueduct. Madden C; Halsted M; Meinzen-Derr J; Bardo D; Boston M; Arjmand E; Nishimura C; Yang T; Benton C; Das V; Smith R; Choo D; Greinwald J Arch Otolaryngol Head Neck Surg; 2007 Feb; 133(2):162-8. PubMed ID: 17309986 [TBL] [Abstract][Full Text] [Related]
19. Hearing loss features in GJB2 biallelic mutations and GJB2/GJB6 digenic inheritance in a large Italian cohort. Cama E; Melchionda S; Palladino T; Carella M; Santarelli R; Genovese E; Benettazzo F; Zelante L; Arslan E Int J Audiol; 2009 Jan; 48(1):12-7. PubMed ID: 19173109 [TBL] [Abstract][Full Text] [Related]
20. [The results of audiological examination of children presenting with sensorineural loss of hearing due to GJB2 gene mutations during the first year of life]. Lalaiants MR; Bliznets EA; Markova TG; Poliakov AV; Tavartkiladze GA Vestn Otorinolaringol; 2011; (3):31-5. PubMed ID: 21720291 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]