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 *

47 related articles for article (PubMed ID: 31487726)

  • 1. Genetics of Hereditary Hearing Loss in the Middle East: A Systematic Review of the Carrier Frequency of the GJB2 Mutation (35delG).
    Koohiyan M
    Audiol Neurootol; 2019; 24(4):161-165. PubMed ID: 31487726
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Statistical study of 35delG mutation of GJB2 gene: a meta-analysis of carrier frequency.
    Mahdieh N; Rabbani B
    Int J Audiol; 2009; 48(6):363-70. PubMed ID: 19925344
    [TBL] [Abstract][Full Text] [Related]  

  • 3. High carrier frequency of the GJB2 mutation (35delG) in the north of Iran.
    Chaleshtori MH; Farrokhi E; Shahrani M; Kheiri S; Dolati M; Rad LH; Pour-Jafari H; Samani KG; Chaleshtori KS; Crosby AH
    Int J Pediatr Otorhinolaryngol; 2007 Jun; 71(6):863-7. PubMed ID: 17428550
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Updated carrier rates for c.35delG (GJB2) associated with hearing loss in Russia and common c.35delG haplotypes in Siberia.
    Zytsar MV; Barashkov NA; Bady-Khoo MS; Shubina-Olejnik OA; Danilenko NG; Bondar AA; Morozov IV; Solovyev AV; Danilchenko VY; Maximov VN; Posukh OL
    BMC Med Genet; 2018 Aug; 19(1):138. PubMed ID: 30086704
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genetics of hereditary hearing loss in east Iran population: A systematic review of
    Koohiyan M; Azadegan-Dehkordi F; Koohian F; Abolhasani M; Hashemzadeh-Chaleshtori M
    Intractable Rare Dis Res; 2019 Aug; 8(3):172-178. PubMed ID: 31523594
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Prevalence of the c.35delG and p.W24X mutations in the GJB2 gene in patients with nonsyndromic hearing loss from North-West Romania.
    Lazăr C; Popp R; Trifa A; Mocanu C; Mihut G; Al-Khzouz C; Tomescu E; Figan I; Grigorescu-Sido P
    Int J Pediatr Otorhinolaryngol; 2010 Apr; 74(4):351-5. PubMed ID: 20096468
    [TBL] [Abstract][Full Text] [Related]  

  • 7. GJB2 (Connexin-26) mutations are not frequent among hearing impaired patients in east Greenland.
    Homøe P; Koch A; Rendtorff ND; Lodahl M; Andersen T; Andersen S; Eiberg H; Nielsen IM; Tranebjærg L
    Int J Audiol; 2012 Jun; 51(6):433-6. PubMed ID: 22369226
    [TBL] [Abstract][Full Text] [Related]  

  • 8. [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]  

  • 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. Carrier frequency of GJB2 gene mutations c.35delG, c.235delC and c.167delT among the populations of Eurasia.
    Dzhemileva LU; Barashkov NA; Posukh OL; Khusainova RI; Akhmetova VL; Kutuev IA; Gilyazova IR; Tadinova VN; Fedorova SA; Khidiyatova IM; Lobov SL; Khusnutdinova EK
    J Hum Genet; 2010 Nov; 55(11):749-54. PubMed ID: 20739944
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The contribution of GJB2 (Connexin 26) 35delG to age-related hearing impairment and noise-induced hearing loss.
    Van Eyken E; Van Laer L; Fransen E; Topsakal V; Hendrickx JJ; Demeester K; Van de Heyning P; Mäki-Torkko E; Hannula S; Sorri M; Jensen M; Parving A; Bille M; Baur M; Pfister M; Bonaconsa A; Mazzoli M; Orzan E; Espeso A; Stephens D; Verbruggen K; Huyghe J; Dhooge I; Huygen P; Kremer H; Cremers C; Kunst S; Manninen M; Pyykkö I; Rajkowska E; Pawelczyk M; Sliwinska-Kowalska M; Steffens M; Wienker T; Van Camp G
    Otol Neurotol; 2007 Oct; 28(7):970-5. PubMed ID: 17909436
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Hypothesizing an ancient Greek origin of the GJB2 35delG mutation: can science meet history?
    Kokotas H; Grigoriadou M; Villamar M; Giannoulia-Karantana A; del Castillo I; Petersen MB
    Genet Test Mol Biomarkers; 2010 Apr; 14(2):183-7. PubMed ID: 20073550
    [TBL] [Abstract][Full Text] [Related]  

  • 13. GJB2 sequencing in deaf and profound sensorineural hearing loss children.
    Mielczarek M; Zakrzewska A; Olszewski J
    Otolaryngol Pol; 2016 Jun; 70(3):21-5. PubMed ID: 27386929
    [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. Evidence for single origins of 35delG and delE120 mutations in the GJB2 gene in Anatolia.
    Tekin M; Boğoclu G; Arican ST; Orman MN; Tastan H; Elsobky E; Elsayed S; Akar N
    Clin Genet; 2005 Jan; 67(1):31-7. PubMed ID: 15617546
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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]  

  • 17. A systematic review of SLC26A4 mutations causing hearing loss in the Iranian population.
    Koohiyan M
    Int J Pediatr Otorhinolaryngol; 2019 Oct; 125():1-5. PubMed ID: 31228605
    [TBL] [Abstract][Full Text] [Related]  

  • 18. The Cause of Hereditary Hearing Loss in
    Safka Brozkova D; Uhrova Meszarosova A; Lassuthova P; Varga L; Staněk D; Borecká S; Laštůvková J; Čejnová V; Rašková D; Lhota F; Gašperíková D; Seeman P
    Genes (Basel); 2021 May; 12(5):. PubMed ID: 34062854
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Systematic Review of Pathogenic GJB2 Variants in the Latino Population.
    Bouzaher MH; Worden CP; Jeyakumar A
    Otol Neurotol; 2020 Feb; 41(2):e182-e191. PubMed ID: 31834214
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Genetics of Hearing Loss in North Iran Population: An Update of Spectrum and Frequency of GJB2 Mutations.
    Koohiyan M; Azadegan-Dehkordi F; Koohian F; Hashemzadeh-Chaleshtori M
    J Audiol Otol; 2019 Oct; 23(4):175-180. PubMed ID: 31569309
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 3.