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 *

125 related articles for article (PubMed ID: 14691997)

  • 1. First report of prenatal diagnosis of genetic congenital deafness in a routine prenatal genetic test.
    Santoro ML; Mobili L; Mesoraca A; Giorlandino C
    Prenat Diagn; 2003 Dec; 23(13):1083-5. PubMed ID: 14691997
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Connexin26 mutations associated with the most common form of non-syndromic neurosensory autosomal recessive deafness (DFNB1) in Mediterraneans.
    Zelante L; Gasparini P; Estivill X; Melchionda S; D'Agruma L; Govea N; Milá M; Monica MD; Lutfi J; Shohat M; Mansfield E; Delgrosso K; Rappaport E; Surrey S; Fortina P
    Hum Mol Genet; 1997 Sep; 6(9):1605-9. PubMed ID: 9285800
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. 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]  

  • 6. 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]  

  • 7. Molecular studies in the GJB2 gene (Cx26) among a deaf population from Bogotá, Colombia: results of a screening program.
    Tamayo ML; Olarte M; Gelvez N; Gómez M; Frías JL; Bernal JE; Florez S; Medina D
    Int J Pediatr Otorhinolaryngol; 2009 Jan; 73(1):97-101. PubMed ID: 19027181
    [TBL] [Abstract][Full Text] [Related]  

  • 8. GJB2 gene mutations in childhood deafness.
    Angeli S; Utrera R; Dib S; Chiossone E; Naranjo C; Henríquez O; Porta M
    Acta Otolaryngol; 2000 Mar; 120(2):133-6. PubMed ID: 11603757
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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]  

  • 10. [Hereditary deafness in Kirov oblast: estimation of the incidence rate and DNA diagnosis in children].
    Zinchenko RA; Osetrova AA; Sharonova EI
    Genetika; 2012 Apr; 48(4):542-50. PubMed ID: 22730774
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Belgian population using an easy and reliable screening method.
    Storm K; Willocx S; Flothmann K; Van Camp G
    Hum Mutat; 1999; 14(3):263-6. PubMed ID: 10477435
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. A seminested PCR test for simultaneous detection of two common mutations (35delG and 167delT) in the connexin-26 gene.
    Simsek M; Al-Wardy N; Al-Khabory M
    Mol Diagn; 2001 Mar; 6(1):63-7. PubMed ID: 11257213
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Significance of heterozygosis M34T mutation of GJB2 gene in non-syndromic congenital deafness. Retrospective analysis of 12,472 samples of amniotic fluid.
    Coco M; Salvinelli F; Greco F; Trivelli M; D'Emidio L; Mesoraca A; Giorlandino C; Raffio R; Coco C
    J Prenat Med; 2013 Oct; 7(4):56-8. PubMed ID: 24611097
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. A simple method of screening for the common connexin-26 gene 35delG mutation in nonsyndromic neurosensory autosomal recessive deafness.
    Fernández-Burriel M; Rodríguez-Quiñones F
    Genet Test; 2003; 7(2):147-9. PubMed ID: 12885338
    [TBL] [Abstract][Full Text] [Related]  

  • 17. A simple PCR test to detect the common 35delG mutation in the connexin 26 gene.
    Wilcox SA; Osborn AH; Dahl HH
    Mol Diagn; 2000 Mar; 5(1):75-8. PubMed ID: 10837093
    [TBL] [Abstract][Full Text] [Related]  

  • 18. [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]  

  • 19. First-trimester prenatal screening for the common 35delG GJB2 mutation causing prelingual deafness.
    Coviello DA; Brambati B; Tului L; Percesepe A; Sironi F; Sahai A; Bertorelli R; Forabosco A
    Prenat Diagn; 2004 Aug; 24(8):631-4. PubMed ID: 15305352
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 7.