BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

879 related articles for article (PubMed ID: 20601923)

  • 1. Prevalence of Connexin 26 (GJB2) and Pendred (SLC26A4) mutations in a population of adult cochlear implant candidates.
    Hochman JB; Stockley TL; Shipp D; Lin VY; Chen JM; Nedzelski JM
    Otol Neurotol; 2010 Aug; 31(6):919-22. PubMed ID: 20601923
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. [Etiologic analysis of severe to profound hearing loss patients from Chifeng city in Inner Mongolia].
    Yuan YY; Dai P; Zhu XH; Kang DY; Zhang X; Huang DL
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2009 Apr; 44(4):292-6. PubMed ID: 19558834
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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]  

  • 5. Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndrome.
    Ben Said M; Dhouib H; BenZina Z; Ghorbel A; Moreno F; Masmoudi S; Ayadi H; Hmani-Aifa M
    Int J Pediatr Otorhinolaryngol; 2012 Jun; 76(6):832-6. PubMed ID: 22429511
    [TBL] [Abstract][Full Text] [Related]  

  • 6. A Novel Mutation in SLC26A4 Causes Nonsyndromic Autosomal Recessive Hearing Impairment.
    Wolf A; Frohne A; Allen M; Parzefall T; Koenighofer M; Schreiner MM; Schoefer C; Frei K; Lucas T
    Otol Neurotol; 2017 Feb; 38(2):173-179. PubMed ID: 27861301
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Spectrum and frequency of GJB2, GJB6 and SLC26A4 gene mutations among nonsyndromic hearing loss patients in eastern part of India.
    Adhikary B; Ghosh S; Paul S; Bankura B; Pattanayak AK; Biswas S; Maity B; Das M
    Gene; 2015 Dec; 573(2):239-45. PubMed ID: 26188157
    [TBL] [Abstract][Full Text] [Related]  

  • 8. 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]  

  • 9. Ethnicity and mutations in GJB2 (connexin 26) and GJB6 (connexin 30) in a multi-cultural Canadian paediatric Cochlear Implant Program.
    Propst EJ; Stockley TL; Gordon KA; Harrison RV; Papsin BC
    Int J Pediatr Otorhinolaryngol; 2006 Mar; 70(3):435-44. PubMed ID: 16125251
    [TBL] [Abstract][Full Text] [Related]  

  • 10. [Analysis of the hereditary etiology of 336 patients with non-syndromic sensorineural hearing loss from Ningxia Hui Autonomous Region of China].
    Wang YL; Zhu YM; Liu XW; Xu BC; Guo YF; Wang QJ
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2012 Sep; 47(9):760-3. PubMed ID: 23141447
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Particular distribution of the GJB2/GJB6 gene mutations in Mexican population with hearing impairment.
    Loeza-Becerra F; Rivera-Vega Mdel R; Martínez-Saucedo M; Gonzalez-Huerta LM; Urueta-Cuellar H; Berrruecos-Villalobos P; Cuevas-Covarrubias S
    Int J Pediatr Otorhinolaryngol; 2014 Jul; 78(7):1057-60. PubMed ID: 24774219
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Prevalence of 35delG/GJB2 and del (GJB6-D13S1830) mutations in patients with non-syndromic deafness from a population of Espírito Santo-Brazil.
    Cordeiro-Silva Mde F; Barbosa A; Santiago M; Provetti M; Rabbi-Bortolini E
    Braz J Otorhinolaryngol; 2010; 76(4):428-32. PubMed ID: 20835527
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. 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]  

  • 16. Molecular analysis of the GJB2, GJB6 and SLC26A4 genes in Korean deafness patients.
    Lee KY; Choi SY; Bae JW; Kim S; Chung KW; Drayna D; Kim UK; Lee SH
    Int J Pediatr Otorhinolaryngol; 2008 Sep; 72(9):1301-9. PubMed ID: 18585793
    [TBL] [Abstract][Full Text] [Related]  

  • 17. GJB2 mutations and additional disabilities in a pediatric cochlear implant population.
    Wiley S; Choo D; Meinzen-Derr J; Hilbert L; Greinwald J
    Int J Pediatr Otorhinolaryngol; 2006 Mar; 70(3):493-500. PubMed ID: 16154643
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Connexin gene mutations among Ugandan patients with nonsyndromic sensorineural hearing loss.
    Javidnia H; Carson N; Awubwa M; Byaruhanga R; Mack D; Vaccani JP
    Laryngoscope; 2014 Sep; 124(9):E373-6. PubMed ID: 24706568
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Prevalence of c.35delG and p.M34T mutations in the GJB2 gene in Estonia.
    Teek R; Kruustük K; Zordania R; Joost K; Reimand T; Möls T; Oitmaa E; Kahre T; Tõnisson N; Ounap K
    Int J Pediatr Otorhinolaryngol; 2010 Sep; 74(9):1007-12. PubMed ID: 20708129
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [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]  

    [Next]    [New Search]
    of 44.