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 *

160 related articles for article (PubMed ID: 38605287)

  • 21. Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness.
    Esmaeili M; Bonyadi M; Nejadkazem M
    Int J Pediatr Otorhinolaryngol; 2007 Jun; 71(6):869-73. PubMed ID: 17368814
    [TBL] [Abstract][Full Text] [Related]  

  • 22. 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]  

  • 23. Role of
    Falah M; Houshmand M; Balali M; Asghari A; Bagher Z; Alizadeh R; Farhadi M
    Fetal Pediatr Pathol; 2020 Feb; 39(1):1-12. PubMed ID: 31215297
    [No Abstract]   [Full Text] [Related]  

  • 24. GJB2 and GJB6 screening in Tunisian patients with autosomal recessive deafness.
    Trabelsi M; Bahri W; Habibi M; Zainine R; Maazoul F; Ghazi B; Chaabouni H; Mrad R
    Int J Pediatr Otorhinolaryngol; 2013 May; 77(5):714-6. PubMed ID: 23434199
    [TBL] [Abstract][Full Text] [Related]  

  • 25. [Spectrum of
    Zheng BJ; Zhang T; Wang H; Tang XW; Zheng J; Lv JX; Guan MX
    Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2016 Jun; 30(12):933-937. PubMed ID: 29771057
    [No Abstract]   [Full Text] [Related]  

  • 26. Low incidence of GJB2, GJB6 and mitochondrial DNA mutations in North Indian patients with non-syndromic hearing impairment.
    Bhalla S; Sharma R; Khandelwal G; Panda NK; Khullar M
    Biochem Biophys Res Commun; 2009 Jul; 385(3):445-8. PubMed ID: 19465004
    [TBL] [Abstract][Full Text] [Related]  

  • 27. 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]  

  • 28. Longitudinal phenotypic analysis in patients with connexin 26 (GJB2) (DFNB1) and connexin 30 (GJB6) mutations.
    Stinckens C; Kremer H; van Wijk E; Hoefsloot LH; Huygen PL; Standaert L; Fryns JP; Cremers CW
    Ann Otol Rhinol Laryngol; 2004 Jul; 113(7):587-93. PubMed ID: 15274422
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Molecular screening of deafness in Algeria: high genetic heterogeneity involving DFNB1 and the Usher loci, DFNB2/USH1B, DFNB12/USH1D and DFNB23/USH1F.
    Ammar-Khodja F; Faugère V; Baux D; Giannesini C; Léonard S; Makrelouf M; Malek R; Djennaoui D; Zenati A; Claustres M; Roux AF
    Eur J Med Genet; 2009; 52(4):174-9. PubMed ID: 19375528
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Unique spectrum of GJB2 mutations in Mexico.
    de la Luz Arenas-Sordo M; Menendez I; Hernández-Zamora E; Sirmaci A; Gutiérrez-Tinajero D; McGetrick M; Murphy-Ruiz P; Leyva-Juárez X; Huesca-Hernández F; Dominguez-Aburto J; Tekin M
    Int J Pediatr Otorhinolaryngol; 2012 Nov; 76(11):1678-80. PubMed ID: 22925408
    [TBL] [Abstract][Full Text] [Related]  

  • 32. DFNB1-associated deafness in Portuguese cochlear implant users: prevalence and impact on oral outcome.
    Chora JR; Matos TD; Martins JH; Alves MC; Andrade SM; Silva LF; Ribeiro CA; Antunes MC; Fialho MG; Caria MH
    Int J Pediatr Otorhinolaryngol; 2010 Oct; 74(10):1135-9. PubMed ID: 20650534
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Mutation spectrum of autosomal recessive non-syndromic hearing loss in central Iran.
    Haghighat-Nia A; Keivani A; Nadeali Z; Fazel-Najafabadi E; Hosseinzadeh M; Salehi M
    Int J Pediatr Otorhinolaryngol; 2015 Nov; 79(11):1892-5. PubMed ID: 26409293
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Prevalence of mutations located at the dfnb1 locus in a population of cochlear implanted children in eastern Romania.
    Rădulescu L; Mârţu C; Birkenhäger R; Cozma S; Ungureanu L; Laszig R
    Int J Pediatr Otorhinolaryngol; 2012 Jan; 76(1):90-4. PubMed ID: 22070872
    [TBL] [Abstract][Full Text] [Related]  

  • 35. GJB2 mutations in hearing impairment: identification of a broad clinical spectrum for improved genetic counseling.
    Frei K; Ramsebner R; Lucas T; Hamader G; Szuhai K; Weipoltshammer K; Baumgartner WD; Wachtler FJ; Kirschhofer K
    Laryngoscope; 2005 Mar; 115(3):461-5. PubMed ID: 15744158
    [TBL] [Abstract][Full Text] [Related]  

  • 36. A novel DFNB1 deletion allele supports the existence of a distant cis-regulatory region that controls GJB2 and GJB6 expression.
    Wilch E; Azaiez H; Fisher RA; Elfenbein J; Murgia A; Birkenhäger R; Bolz H; Da Silva-Costa SM; Del Castillo I; Haaf T; Hoefsloot L; Kremer H; Kubisch C; Le Marechal C; Pandya A; Sartorato EL; Schneider E; Van Camp G; Wuyts W; Smith RJ; Friderici KH
    Clin Genet; 2010 Sep; 78(3):267-74. PubMed ID: 20236118
    [TBL] [Abstract][Full Text] [Related]  

  • 37. 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]  

  • 38.
    Tingang Wonkam E; Chimusa E; Noubiap JJ; Adadey SM; F Fokouo JV; Wonkam A
    Genes (Basel); 2019 Oct; 10(11):. PubMed ID: 31731535
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Analysis of the presence of the GJB6 mutations in patients heterozygous for GJB2 mutation in Brazil.
    Esteves MC; de Lima Isaac M; Francisco AM; da Silva Junior WA; Ferreira CA; Dell'Aringa AH
    Eur Arch Otorhinolaryngol; 2014 Apr; 271(4):695-9. PubMed ID: 23553242
    [TBL] [Abstract][Full Text] [Related]  

  • 40. A new large deletion in the DFNB1 locus causes nonsyndromic hearing loss.
    Feldmann D; Le Maréchal C; Jonard L; Thierry P; Czajka C; Couderc R; Ferec C; Denoyelle F; Marlin S; Fellmann F
    Eur J Med Genet; 2009; 52(4):195-200. PubMed ID: 19101659
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.