These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

115 related articles for article (PubMed ID: 32553771)

  • 1. Differences in hearing levels between siblings with hearing loss caused by GJB2 mutations.
    Fujioka M; Hosoya M; Nara K; Morimoto N; Sakamoto H; Otsu M; Nakano A; Arimoto Y; Masuda S; Sugiuchi T; Masuda S; Morita N; Ogawa K; Kaga K; Matsunaga T
    Auris Nasus Larynx; 2020 Dec; 47(6):938-942. PubMed ID: 32553771
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Investigation of the hearing levels of siblings affected by a single GJB2 variant: Possibility of genetic modifiers.
    Hosoya M; Fujioka M; Nara K; Morimoto N; Masuda S; Sugiuchi T; Katsunuma S; Takagi A; Morita N; Ogawa K; Kaga K; Matsunaga T
    Int J Pediatr Otorhinolaryngol; 2021 Oct; 149():110840. PubMed ID: 34293626
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Does universal newborn hearing screening identify all children with GJB2 (Connexin 26) deafness? Penetrance of GJB2 deafness.
    Norris VW; Arnos KS; Hanks WD; Xia X; Nance WE; Pandya A
    Ear Hear; 2006 Dec; 27(6):732-41. PubMed ID: 17086082
    [TBL] [Abstract][Full Text] [Related]  

  • 4. A genotype-phenotype correlation for GJB2 (connexin 26) deafness.
    Cryns K; Orzan E; Murgia A; Huygen PL; Moreno F; del Castillo I; Chamberlin GP; Azaiez H; Prasad S; Cucci RA; Leonardi E; Snoeckx RL; Govaerts PJ; Van de Heyning PH; Van de Heyning CM; Smith RJ; Van Camp G
    J Med Genet; 2004 Mar; 41(3):147-54. PubMed ID: 14985372
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Clinical phenotype and mutations in connexin 26 (DFNB1/GJB2), the most common cause of childhood hearing loss.
    Cohn ES; Kelley PM
    Am J Med Genet; 1999 Sep; 89(3):130-6. PubMed ID: 10704187
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Effects of GJB2 genotypes on the audiological phenotype: variability is present for all genotypes.
    Hişmi BO; Yilmaz ST; Incesulu A; Tekin M
    Int J Pediatr Otorhinolaryngol; 2006 Oct; 70(10):1687-94. PubMed ID: 16712961
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. Prevalence of DFNB1 mutations in Argentinean children with non-syndromic deafness. Report of a novel mutation in GJB2.
    Gravina LP; Foncuberta ME; Prieto ME; Garrido J; Barreiro C; Chertkoff L
    Int J Pediatr Otorhinolaryngol; 2010 Mar; 74(3):250-4. PubMed ID: 20022641
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. A novel p.Leu213X mutation in GJB2 gene in a Portuguese family.
    Gonçalves AC; Chora J; Matos TD; Santos R; O'Neill A; Escada P; Fialho G; Caria H
    Int J Pediatr Otorhinolaryngol; 2013 Jan; 77(1):89-91. PubMed ID: 23141775
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Prevalence of GJB2 Mutations in Affected Individuals from United Arab Emirates with Autosomal Recessive Nonsyndromic Hearing Loss.
    Tlili A; Al Mutery A; Kamal Eddine Ahmad Mohamed W; Mahfood M; Hadj Kacem H
    Genet Test Mol Biomarkers; 2017 Nov; 21(11):686-691. PubMed ID: 29016196
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Connexin-26-associated deafness: phenotypic variability and progression of hearing loss.
    Chan DK; Schrijver I; Chang KW
    Genet Med; 2010 Mar; 12(3):174-81. PubMed ID: 20154630
    [TBL] [Abstract][Full Text] [Related]  

  • 14. GJB2-associated hearing loss undetected by hearing screening of newborns.
    Minami SB; Mutai H; Nakano A; Arimoto Y; Taiji H; Morimoto N; Sakata H; Adachi N; Masuda S; Sakamoto H; Yoshida H; Tanaka F; Morita N; Sugiuchi T; Kaga K; Matsunaga T
    Gene; 2013 Dec; 532(1):41-5. PubMed ID: 24013081
    [TBL] [Abstract][Full Text] [Related]  

  • 15. The controversial p.Met34Thr variant in GJB2 gene: Two siblings, one genotype, two phenotypes.
    Lameiras AR; Gonçalves AC; Santos R; O'Neill A; Reis LR; Matos TD; Fialho G; Caria H; Escada P
    Int J Pediatr Otorhinolaryngol; 2015 Aug; 79(8):1316-9. PubMed ID: 26117665
    [TBL] [Abstract][Full Text] [Related]  

  • 16. [Non-invasive screening for GJB2 mutations in buccal smears for the diagnosis of inherited hearing impairment].
    Schade G; Kothe C; Ruge G; Hess M; Meyer CG
    Laryngorhinootologie; 2003 Jun; 82(6):397-401. PubMed ID: 12851846
    [TBL] [Abstract][Full Text] [Related]  

  • 17. GJB2 sequencing in deaf and profound sensorineural hearing loss children.
    Mielczarek M; Zakrzewska A; Olszewski J
    Otolaryngol Pol; 2016 Jun; 70(3):21-5. PubMed ID: 27386929
    [TBL] [Abstract][Full Text] [Related]  

  • 18. GJB2 mutation spectrum in the Taiwanese population and genotype-phenotype comparisons in patients with hearing loss carrying GJB2 c.109G>A and c.235delC mutations.
    Lin YF; Lin HC; Tsai CL; Hsu YC
    Hear Res; 2022 Jan; 413():108135. PubMed ID: 33288323
    [TBL] [Abstract][Full Text] [Related]  

  • 19. 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]  

  • 20. [The mutation spectrum of the GJB2 gene in Belarussian patients with hearing loss. Results of pilot genetic screening of hearing impairment in newborns].
    Bliznets EA; Marcul' DN; Khorov OG; Markova TG; Poliakov AV
    Genetika; 2014 Feb; 50(2):214-21. PubMed ID: 25711030
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 6.