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5. Correlation analysis of phenotype and genotype of GJB2 in patients with non-syndromic hearing loss in China. Dai ZY; Sun BC; Huang SS; Yuan YY; Zhu YH; Su Y; Dai P Gene; 2015 Oct; 570(2):272-6. PubMed ID: 26095810 [TBL] [Abstract][Full Text] [Related]
6. Identification and genotype/phenotype correlation of mutations in a large German cohort with hearing loss. Beck C; Pérez-Álvarez JC; Sigruener A; Haubner F; Seidler T; Aslanidis C; Strutz J; Schmitz G Eur Arch Otorhinolaryngol; 2015 Oct; 272(10):2765-76. PubMed ID: 25214170 [TBL] [Abstract][Full Text] [Related]
7. Newborn genetic screening for hearing impairment: a population-based longitudinal study. Wu CC; Tsai CH; Hung CC; Lin YH; Lin YH; Huang FL; Tsao PN; Su YN; Lee YL; Hsieh WS; Hsu CJ Genet Med; 2017 Jan; 19(1):6-12. PubMed ID: 27308839 [TBL] [Abstract][Full Text] [Related]
8. GJB2 Mutation Spectrum and Genotype-Phenotype Correlation in 1067 Han Chinese Subjects with Non-Syndromic Hearing Loss. Zheng J; Ying Z; Cai Z; Sun D; He Z; Gao Y; Zhang T; Zhu Y; Chen Y; Guan MX PLoS One; 2015; 10(6):e0128691. PubMed ID: 26043044 [TBL] [Abstract][Full Text] [Related]
9. Phenotype-genotype correlation in 295 Chinese deaf subjects with biallelic causative mutations in the GJB2 gene. Zhao FF; Ji YB; Wang DY; Lan L; Han MK; Li Q; Zhao Y; Rao S; Han D; Wang QJ Genet Test Mol Biomarkers; 2011 Sep; 15(9):619-25. PubMed ID: 21488715 [TBL] [Abstract][Full Text] [Related]
10. Audiological features of GJB2 (connexin 26) deafness. Liu XZ; Pandya A; Angeli S; Telischi FF; Arnos KS; Nance WE; Balkany T Ear Hear; 2005 Jun; 26(3):361-9. PubMed ID: 15937416 [TBL] [Abstract][Full Text] [Related]
11. The Relationship between the p.V37I Mutation in GJB2 and Hearing Phenotypes in Chinese Individuals. Huang S; Huang B; Wang G; Yuan Y; Dai P PLoS One; 2015; 10(6):e0129662. PubMed ID: 26061099 [TBL] [Abstract][Full Text] [Related]
13. Hearing impairment in Dutch patients with connexin 26 (GJB2) and connexin 30 (GJB6) mutations. Santos RL; Aulchenko YS; Huygen PL; van der Donk KP; de Wijs IJ; Kemperman MH; Admiraal RJ; Kremer H; Hoefsloot LH; Cremers CW Int J Pediatr Otorhinolaryngol; 2005 Feb; 69(2):165-74. PubMed ID: 15656949 [TBL] [Abstract][Full Text] [Related]
14. Clinical course of hearing and language development in GJB2 and non-GJB2 deafness following habilitation with hearing aids. Matsunaga T; Hirota E; Bito S; Niimi S; Usami S Audiol Neurootol; 2006; 11(1):59-68. PubMed ID: 16282682 [TBL] [Abstract][Full Text] [Related]
15. Prevalence of GJB2 (connexin-26) and GJB6 (connexin-30) mutations in a cohort of 300 Brazilian hearing-impaired individuals: implications for diagnosis and genetic counseling. Batissoco AC; Abreu-Silva RS; Braga MC; Lezirovitz K; Della-Rosa V; Alfredo T; Otto PA; Mingroni-Netto RC Ear Hear; 2009 Feb; 30(1):1-7. PubMed ID: 19125024 [TBL] [Abstract][Full Text] [Related]
16. A large cohort study of GJB2 mutations in Japanese hearing loss patients. Tsukada K; Nishio S; Usami S; Clin Genet; 2010 Nov; 78(5):464-70. PubMed ID: 20497192 [TBL] [Abstract][Full Text] [Related]
17. Analysis of p.V37I compound heterozygous mutations in the GJB2 gene in Chinese infants and young children. Du Y; Huang L; Cheng X; Zhao L; Ruan Y; Ni T Biosci Trends; 2016 Jul; 10(3):220-6. PubMed ID: 27350192 [TBL] [Abstract][Full Text] [Related]
18. GJB2 mutations in the Swiss hearing impaired. Gürtler N; Kim Y; Mhatre A; Müller R; Probst R; Lalwani AK Ear Hear; 2003 Oct; 24(5):440-7. PubMed ID: 14534413 [TBL] [Abstract][Full Text] [Related]
19. [Analysis of GJB2 gene coding sequence in patients with nonsyndromic hearing loss]. Sun SC; Liu YX; Peng YS; Li HF; Xie CY Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Aug; 28(4):409-13. PubMed ID: 21811981 [TBL] [Abstract][Full Text] [Related]
20. 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] [Next] [New Search]