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 *

121 related articles for article (PubMed ID: 10204859)

  • 1. Allele specific oligonucleotide analysis of the common deafness mutation 35delG in the connexin 26 (GJB2) gene.
    Rabionet R; Estivill X
    J Med Genet; 1999 Mar; 36(3):260-1. PubMed ID: 10204859
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Connexin-26 mutations in sporadic and inherited sensorineural deafness.
    Estivill X; Fortina P; Surrey S; Rabionet R; Melchionda S; D'Agruma L; Mansfield E; Rappaport E; Govea N; Milà M; Zelante L; Gasparini P
    Lancet; 1998 Feb; 351(9100):394-8. PubMed ID: 9482292
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. Strong linkage disequilibrium for the frequent GJB2 35delG mutation in the Greek population.
    Kokotas H; Van Laer L; Grigoriadou M; Iliadou V; Economides J; Pomoni S; Pampanos A; Eleftheriades N; Ferekidou E; Korres S; Giannoulia-Karantana A; Van Camp G; Petersen MB
    Am J Med Genet A; 2008 Nov; 146A(22):2879-84. PubMed ID: 18925674
    [TBL] [Abstract][Full Text] [Related]  

  • 5. The prevalence of connexin 26 ( GJB2) mutations in the Chinese population.
    Liu XZ; Xia XJ; Ke XM; Ouyang XM; Du LL; Liu YH; Angeli S; Telischi FF; Nance WE; Balkany T; Xu LR
    Hum Genet; 2002 Oct; 111(4-5):394-7. PubMed ID: 12384781
    [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. 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]  

  • 8. 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]  

  • 9. High carrier frequency of the 35delG deafness mutation in European populations. Genetic Analysis Consortium of GJB2 35delG.
    Gasparini P; Rabionet R; Barbujani G; Melçhionda S; Petersen M; Brøndum-Nielsen K; Metspalu A; Oitmaa E; Pisano M; Fortina P; Zelante L; Estivill X
    Eur J Hum Genet; 2000 Jan; 8(1):19-23. PubMed ID: 10713883
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Spectrum and frequencies of mutations in the GJB2 (Cx26) gene among 156 Czech patients with pre-lingual deafness.
    Seeman P; Malíková M; Rasková D; Bendová O; Groh D; Kubálková M; Sakmaryová I; Seemanová E; Kabelka Z
    Clin Genet; 2004 Aug; 66(2):152-7. PubMed ID: 15253766
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. 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]  

  • 13. The 35delG mutation in the connexin 26 gene (GJB2) associated with congenital deafness: European carrier frequencies and evidence for its origin in ancient Greece.
    Lucotte G; Diéterlen F
    Genet Test; 2005; 9(1):20-5. PubMed ID: 15857182
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Determination of the carrier frequency of the common GJB2 (connexin-26) 35delG mutation in the Greek Cypriot population.
    Neocleous V; Portides G; Anastasiadou V; Phylactou LA
    Int J Pediatr Otorhinolaryngol; 2006 Aug; 70(8):1473-7. PubMed ID: 16713631
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. 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]  

  • 17. Connexin 26 35delG does not represent a mutational hotspot.
    Rothrock CR; Murgia A; Sartorato EL; Leonardi E; Wei S; Lebeis SL; Yu LE; Elfenbein JL; Fisher RA; Friderici KH
    Hum Genet; 2003 Jul; 113(1):18-23. PubMed ID: 12684873
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Frequency of the 35delG allele causing nonsyndromic recessive deafness in the Algerian patients.
    Ammar-Khodja F; Makrelouf M; Malek R; Ibrahim H; Zenati A
    Genet Couns; 2007; 18(4):383-91. PubMed ID: 18286819
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Carrier frequencies of mutations/polymorphisms in the connexin 26 gene (GJB2) in the Moroccan population.
    Abidi O; Boulouiz R; Nahili H; Bakhouch K; Wakrim L; Rouba H; Chafik A; Hassar M; Barakat A
    Genet Test; 2008 Dec; 12(4):569-74. PubMed ID: 19072567
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.