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 *

498 related articles for article (PubMed ID: 12176179)

  • 1. 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]  

  • 2. Prelingual nonsyndromic hearing loss in Greece. Molecular and clinical findings.
    Iliades T; Eleftheriades N; Iliadou V; Pampanos A; Voyiatzis N; Economides J; Leotsakos P; Neou P; Tsakanikos M; Antoniadi T; Konstantopoulou I; Yannoukakos D; Grigoriadou M; Skevas A; Petersen MB
    ORL J Otorhinolaryngol Relat Spec; 2002; 64(5):321-3. PubMed ID: 12417772
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. [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]  

  • 6. Prevalence of GBJ2 mutations in patients with severe to profound congenital nonsyndromic sensorineural hearing loss in Bulgarian population.
    Popova DP; Kaneva R; Varbanova S; Popov TM
    Eur Arch Otorhinolaryngol; 2012 Jun; 269(6):1589-92. PubMed ID: 22037723
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Prenatal diagnosis of prelingual deafness: carrier testing and prenatal diagnosis of the common GJB2 35delG mutation.
    Antoniadi T; Pampanos A; Petersen MB
    Prenat Diagn; 2001 Jan; 21(1):10-3. PubMed ID: 11180233
    [TBL] [Abstract][Full Text] [Related]  

  • 8. The novel c.247_249delTTC (p.F83del) GJB2 mutation in a family with prelingual sensorineural deafness.
    Petersen MB; Grigoriadou M; Koutroumpe M; Kokotas H
    Int J Pediatr Otorhinolaryngol; 2012 Jul; 76(7):969-71. PubMed ID: 22484064
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Spectrum and frequency of GJB2 mutations causing deafness in the northwest of Iran.
    Bonyadi MJ; Fotouhi N; Esmaeili M
    Int J Pediatr Otorhinolaryngol; 2014 Apr; 78(4):637-40. PubMed ID: 24529908
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Mutation analysis of GJB2 and GJB6 genes in Southeastern Brazilians with hereditary nonsyndromic deafness.
    Cordeiro-Silva Mde F; Barbosa A; Santiago M; Provetti M; Dettogni RS; Tovar TT; Rabbi-Bortolini E; Louro ID
    Mol Biol Rep; 2011 Feb; 38(2):1309-13. PubMed ID: 20563649
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. GJB2 (Cx26) gene mutations in Chinese patients with congenital sensorineural deafness and a report of one novel mutation.
    Xiao ZA; Xie DH
    Chin Med J (Engl); 2004 Dec; 117(12):1797-801. PubMed ID: 15603707
    [TBL] [Abstract][Full Text] [Related]  

  • 13. 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]  

  • 14. A novel frameshift mutation (c.405delC) in the GJB2 gene associated with autosomal recessive hearing loss in two Tunisian families.
    Riahi Z; Chahed H; Jaafoura H; Zainine R; Messaoud O; Naili M; Nagara M; Hammami H; Laroussi N; Bouyacoub Y; Kefi R; Bonnet C; Besbes G; Abdelhak S
    Int J Pediatr Otorhinolaryngol; 2013 Sep; 77(9):1485-8. PubMed ID: 23856379
    [TBL] [Abstract][Full Text] [Related]  

  • 15. A deletion involving the connexin 30 gene in nonsyndromic hearing impairment.
    del Castillo I; Villamar M; Moreno-Pelayo MA; del Castillo FJ; Alvarez A; Tellería D; Menéndez I; Moreno F
    N Engl J Med; 2002 Jan; 346(4):243-9. PubMed ID: 11807148
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. 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]  

  • 18. 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]  

  • 19. Mutations of the Connexin 26 gene in families with non-syndromic hearing loss.
    Al-Achkar W; Moassass F; Al-Halabi B; Al-Ablog A
    Mol Med Rep; 2011; 4(2):331-5. PubMed ID: 21468573
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Molecular basis of childhood deafness resulting from mutations in the GJB2 (connexin 26) gene.
    Rabionet R; Zelante L; López-Bigas N; D'Agruma L; Melchionda S; Restagno G; Arbonés ML; Gasparini P; Estivill X
    Hum Genet; 2000 Jan; 106(1):40-4. PubMed ID: 10982180
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 25.