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 *

194 related articles for article (PubMed ID: 17036313)

  • 41. Prevalence of GJB2 mutations in prelingual deafness in the Greek population.
    Pampanos A; Economides J; Iliadou V; Neou P; Leotsakos P; Voyiatzis N; Eleftheriades N; Tsakanikos M; Antoniadi T; Hatzaki A; Konstantopoulou I; Yannoukakos D; Gronskov K; Brondum-Nielsen K; Grigoriadou M; Gyftodimou J; Iliades T; Skevas A; Petersen MB
    Int J Pediatr Otorhinolaryngol; 2002 Sep; 65(2):101-8. PubMed ID: 12176179
    [TBL] [Abstract][Full Text] [Related]  

  • 42. 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]  

  • 43. Carrier rates in the midwestern United States for GJB2 mutations causing inherited deafness.
    Green GE; Scott DA; McDonald JM; Woodworth GG; Sheffield VC; Smith RJ
    JAMA; 1999 Jun; 281(23):2211-6. PubMed ID: 10376574
    [TBL] [Abstract][Full Text] [Related]  

  • 44. 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]  

  • 45. Prevalence of GJB2 mutations and the del(GJB6-D13S1830) in Argentinean non-syndromic deaf patients.
    Dalamón V; Béhèran A; Diamante F; Pallares N; Diamante V; Elgoyhen AB
    Hear Res; 2005 Sep; 207(1-2):43-9. PubMed ID: 15964725
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Diagnostic yield in the workup of congenital sensorineural hearing loss is dependent on patient ethnicity.
    Chan DK; Schrijver I; Chang KW
    Otol Neurotol; 2011 Jan; 32(1):81-7. PubMed ID: 21042228
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Hearing loss associated with 35delG mutation in Connexin-26 (GJB2) gene: audiogram analysis.
    Salvinelli F; Casale M; D'Ascanio L; Firrisi L; Greco F; Baldi A
    J Laryngol Otol; 2004 Jan; 118(1):8-11. PubMed ID: 14979964
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Mutations of Cx26 gene (GJB2) for prelingual deafness in Taiwan.
    Wang YC; Kung CY; Su MC; Su CC; Hsu HM; Tsai CC; Lin CC; Li SY
    Eur J Hum Genet; 2002 Aug; 10(8):495-8. PubMed ID: 12111646
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Mutation analysis of the GJB2 (connexin 26) gene by DGGE in Greek patients with sensorineural deafness.
    Antoniadi T; Grønskov K; Sand A; Pampanos A; Brøndum-Nielsen K; Petersen MB
    Hum Mutat; 2000; 16(1):7-12. PubMed ID: 10874298
    [TBL] [Abstract][Full Text] [Related]  

  • 50. GJB2 mutations and degree of hearing loss: a multicenter study.
    Snoeckx RL; Huygen PL; Feldmann D; Marlin S; Denoyelle F; Waligora J; Mueller-Malesinska M; Pollak A; Ploski R; Murgia A; Orzan E; Castorina P; Ambrosetti U; Nowakowska-Szyrwinska E; Bal J; Wiszniewski W; Janecke AR; Nekahm-Heis D; Seeman P; Bendova O; Kenna MA; Frangulov A; Rehm HL; Tekin M; Incesulu A; Dahl HH; du Sart D; Jenkins L; Lucas D; Bitner-Glindzicz M; Avraham KB; Brownstein Z; del Castillo I; Moreno F; Blin N; Pfister M; Sziklai I; Toth T; Kelley PM; Cohn ES; Van Maldergem L; Hilbert P; Roux AF; Mondain M; Hoefsloot LH; Cremers CW; Löppönen T; Löppönen H; Parving A; Gronskov K; Schrijver I; Roberson J; Gualandi F; Martini A; Lina-Granade G; Pallares-Ruiz N; Correia C; Fialho G; Cryns K; Hilgert N; Van de Heyning P; Nishimura CJ; Smith RJ; Van Camp G
    Am J Hum Genet; 2005 Dec; 77(6):945-57. PubMed ID: 16380907
    [TBL] [Abstract][Full Text] [Related]  

  • 51. Update of the spectrum of GJB2 gene mutations in Tunisian families with autosomal recessive nonsyndromic hearing loss.
    Riahi Z; Hammami H; Ouragini H; Messai H; Zainine R; Bouyacoub Y; Romdhane L; Essaid D; Kefi R; Rhimi M; Bedoui M; Dhaouadi A; Feldmann D; Jonard L; Besbes G; Abdelhak S
    Gene; 2013 Aug; 525(1):1-4. PubMed ID: 23680645
    [TBL] [Abstract][Full Text] [Related]  

  • 52. GJB2 c.-23+1G>A mutation is second most common mutation among Iranian individuals with autosomal recessive hearing loss.
    Zeinali S; Davoudi-Dehaghani E; Azadmehr S; DabbaghBagheri S; Bagherian H; Jamali M; Zafarghandimotlagh F; Masoodifard M; BandehiSarhaddi A; Rejali L; Sahebi S
    Eur Arch Otorhinolaryngol; 2015 Sep; 272(9):2255-9. PubMed ID: 25012701
    [TBL] [Abstract][Full Text] [Related]  

  • 53. [Frequency of the Connexin26/35delG mutation and its characteristic phenotype in patients with hearing impairment and controls in Northeastern Hungary].
    Tóth T; Kupka S; Blin N; Pfister M; Sziklai I
    Orv Hetil; 2002 Oct; 143(40):2285-9. PubMed ID: 12420583
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Prevalence and range of GJB2 and SLC26A4 mutations in patients with autosomal recessive non‑syndromic hearing loss.
    Jiang H; Chen J; Shan XJ; Li Y; He JG; Yang BB
    Mol Med Rep; 2014 Jul; 10(1):379-86. PubMed ID: 24737404
    [TBL] [Abstract][Full Text] [Related]  

  • 55. [Pseudodominants of two recessive connexin mutations in non-syndromic sensorineural hearing loss?].
    Birkenhäger R; Zimmer AJ; Maier W; Schipper J
    Laryngorhinootologie; 2006 Mar; 85(3):191-6. PubMed ID: 16547895
    [TBL] [Abstract][Full Text] [Related]  

  • 56. 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]  

  • 57. Cx26 gene mutations in idiopathic progressive hearing loss.
    Ravecca F; Berrettini S; Forli F; Marcaccini M; Casani A; Baldinotti F; Fogli A; Siciliano G; Simi P
    J Otolaryngol; 2005 Apr; 34(2):126-34. PubMed ID: 16076412
    [TBL] [Abstract][Full Text] [Related]  

  • 58. Prevalence of GJB2 (CX26) gene mutations in south Iranian patients with autosomal recessive nonsyndromic sensorineural hearing loss.
    Hashemi SB; Ashraf MJ; Saboori M; Azarpira N; Darai M
    Mol Biol Rep; 2012 Dec; 39(12):10481-7. PubMed ID: 23073770
    [TBL] [Abstract][Full Text] [Related]  

  • 59. Moderate hearing loss and pseudodominant inheritance due to L90P/35delG mutations in the GJB2 (connexin 26) gene.
    Tekin M; Duman T; Boğoçlu G; Incesulu A; Cin S; Akar N
    Genet Couns; 2003; 14(4):379-86. PubMed ID: 14738110
    [TBL] [Abstract][Full Text] [Related]  

  • 60. Autosomal recessive and sporadic deafness in Morocco: high frequency of the 35delG GJB2 mutation and absence of the 342-kb GJB6 variant.
    Gazzaz B; Weil D; Raïs L; Akhyat O; Azeddoug H; Nadifi S
    Hear Res; 2005 Dec; 210(1-2):80-4. PubMed ID: 16243461
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 10.