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 *

143 related articles for article (PubMed ID: 38486023)

  • 1. The congenital hearing phenotype in GJB2 in Queensland, Australia: V37I and mild hearing loss predominates.
    Kriukelis R; Gabbett MT; Beswick R; McInerney-Leo AM; Driscoll C; Liddle K
    Eur J Hum Genet; 2024 Mar; ():. PubMed ID: 38486023
    [TBL] [Abstract][Full Text] [Related]  

  • 2. The contribution of GJB2 mutations to slight or mild hearing loss in Australian elementary school children.
    Dahl HH; Tobin SE; Poulakis Z; Rickards FW; Xu X; Gillam L; Williams J; Saunders K; Cone-Wesson B; Wake M
    J Med Genet; 2006 Nov; 43(11):850-5. PubMed ID: 16840571
    [TBL] [Abstract][Full Text] [Related]  

  • 3. GJB2 and GJB6 mutations: genotypic and phenotypic correlations in a large cohort of hearing-impaired patients.
    Marlin S; Feldmann D; Blons H; Loundon N; Rouillon I; Albert S; Chauvin P; Garabédian EN; Couderc R; Odent S; Joannard A; Schmerber S; Delobel B; Leman J; Journel H; Catros H; Lemarechal C; Dollfus H; Eliot MM; Delaunoy JL; David A; Calais C; Drouin-Garraud V; Obstoy MF; Goizet C; Duriez F; Fellmann F; Hélias J; Vigneron J; Montaut B; Matin-Coignard D; Faivre L; Baumann C; Lewin P; Petit C; Denoyelle F
    Arch Otolaryngol Head Neck Surg; 2005 Jun; 131(6):481-7. PubMed ID: 15967879
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Particular distribution of the GJB2/GJB6 gene mutations in Mexican population with hearing impairment.
    Loeza-Becerra F; Rivera-Vega Mdel R; Martínez-Saucedo M; Gonzalez-Huerta LM; Urueta-Cuellar H; Berrruecos-Villalobos P; Cuevas-Covarrubias S
    Int J Pediatr Otorhinolaryngol; 2014 Jul; 78(7):1057-60. PubMed ID: 24774219
    [TBL] [Abstract][Full Text] [Related]  

  • 5. GJB2 (connexin 26) gene mutations in Moroccan patients with autosomal recessive non-syndromic hearing loss and carrier frequency of the common GJB2-35delG mutation.
    Abidi O; Boulouiz R; Nahili H; Ridal M; Alami MN; Tlili A; Rouba H; Masmoudi S; Chafik A; Hassar M; Barakat A
    Int J Pediatr Otorhinolaryngol; 2007 Aug; 71(8):1239-45. PubMed ID: 17553572
    [TBL] [Abstract][Full Text] [Related]  

  • 6. V37I connexin 26 allele in patients with sensorineural hearing loss: evidence of its pathogenicity.
    Huculak C; Bruyere H; Nelson TN; Kozak FK; Langlois S
    Am J Med Genet A; 2006 Nov; 140(22):2394-400. PubMed ID: 17036313
    [TBL] [Abstract][Full Text] [Related]  

  • 7. GJB2 mutations causing autosomal recessive non-syndromic hearing loss (ARNSHL) in two Iranian populations: Report of two novel variants.
    Koohiyan M; Hashemzadeh-Chaleshtori M; Salehi M; Abtahi H; Reiisi S; Pourreza MR; Noori-Daloii MR; Tabatabaiefar MA
    Int J Pediatr Otorhinolaryngol; 2018 Apr; 107():121-126. PubMed ID: 29501291
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The high frequency of GJB2 gene mutation c.313_326del14 suggests its possible origin in ancestors of Lithuanian population.
    Mikstiene V; Jakaitiene A; Byckova J; Gradauskiene E; Preiksaitiene E; Burnyte B; Tumiene B; Matuleviciene A; Ambrozaityte L; Uktveryte I; Domarkiene I; Rancelis T; Cimbalistiene L; Lesinskas E; Kucinskas V; Utkus A
    BMC Genet; 2016 Feb; 17():45. PubMed ID: 26896187
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. 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]  

  • 11. Prevalence of p.V37I variant of GJB2 among Chinese infants with mild or moderate hearing loss.
    Huang Y; Yang XL; Chen WX; Duan B; Lu P; Wang Y; Xu ZM
    Int J Clin Exp Med; 2015; 8(11):21674-8. PubMed ID: 26885124
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Audiologic and temporal bone imaging findings in patients with sensorineural hearing loss and GJB2 mutations.
    Lee KH; Larson DA; Shott G; Rasmussen B; Cohen AP; Benton C; Halsted M; Choo D; Meinzen-Derr J; Greinwald JH
    Laryngoscope; 2009 Mar; 119(3):554-8. PubMed ID: 19235794
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Distribution and phenotype of GJB2 mutations in 102 Sicilian patients with congenital non syndromic sensorineural hearing loss.
    Salvago P; Martines E; La Mattina E; Mucia M; Sammarco P; Sireci F; Martines F
    Int J Audiol; 2014 Aug; 53(8):558-63. PubMed ID: 24793888
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Hereditary etiology of non-syndromic sensorineural hearing loss in the Republic of North Ossetia-Alania.
    Petrova N; Tebieva I; Kadyshev V; Getoeva Z; Balinova N; Marakhonov A; Vasilyeva T; Ginter E; Kutsev S; Zinchenko R
    PeerJ; 2023; 11():e14514. PubMed ID: 36743950
    [TBL] [Abstract][Full Text] [Related]  

  • 15. GJB2 p.V37I Mutation Associated With Moderate Nonsyndromic Hearing Loss in an Adult Taiwanese Population.
    Yen TT; Chen IC; Cho S; Chang TG; Shih KH; Hua MW; Li JL; Hsu CY; Hsiao TH; Chen YM
    Ear Hear; 2023 Nov-Dec 01; 44(6):1423-1429. PubMed ID: 37271870
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association between the p.V37I variant of GJB2 and hearing loss: a pedigree and meta-analysis.
    Shen N; Peng J; Wang X; Zhu Y; Liu W; Liu A; Lu Y
    Oncotarget; 2017 Jul; 8(28):46681-46690. PubMed ID: 28489599
    [TBL] [Abstract][Full Text] [Related]  

  • 17. First report of prevalence c.IVS1+1G>A and del (GJB6-13S1854) mutations in Syrian families with non-syndromic sensorineural hearing loss.
    Al-Achkar W; Al-Halabi B; Ali B; Moassass F
    Int J Pediatr Otorhinolaryngol; 2017 Jan; 92():82-87. PubMed ID: 28012540
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. GJB2 and GJB6 mutations in 165 Danish patients showing non-syndromic hearing impairment.
    Grønskov K; Larsen LA; Rendtorff ND; Parving A; Nørgaard-Pedersen B; Brøndum-Nielsen K
    Genet Test; 2004; 8(2):181-4. PubMed ID: 15345117
    [TBL] [Abstract][Full Text] [Related]  

  • 20.
    ; ; . PubMed ID:
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 8.