BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

132 related articles for article (PubMed ID: 10353784)

  • 21. Sudden hearing loss in a family with GJB2 related progressive deafness.
    Kokotas H; Theodosiou M; Korres G; Grigoriadou M; Ferekidou E; Giannoulia-Karantana A; Petersen MB; Korres S
    Int J Pediatr Otorhinolaryngol; 2008 Nov; 72(11):1735-40. PubMed ID: 18809215
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Relation between choice of partner and high frequency of connexin-26 deafness.
    Nance WE; Liu XZ; Pandya A
    Lancet; 2000 Aug; 356(9228):500-1. PubMed ID: 10981905
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Common mutation analysis of GJB2 and GJB6 genes in affected families with autosomal recessive non-syndromic hearing loss from Iran: simultaneous detection of two common mutations (35delG/del(GJB6-D13S1830)) in the DFNB1-related deafness.
    Esmaeili M; Bonyadi M; Nejadkazem M
    Int J Pediatr Otorhinolaryngol; 2007 Jun; 71(6):869-73. PubMed ID: 17368814
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Genetic analysis of the connexin-26 M34T variant.
    Griffith AJ
    J Med Genet; 2001 Jul; 38(7):E24. PubMed ID: 11432967
    [No Abstract]   [Full Text] [Related]  

  • 25. 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]  

  • 26. 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]  

  • 27. Molecular screening of deafness in Algeria: high genetic heterogeneity involving DFNB1 and the Usher loci, DFNB2/USH1B, DFNB12/USH1D and DFNB23/USH1F.
    Ammar-Khodja F; Faugère V; Baux D; Giannesini C; Léonard S; Makrelouf M; Malek R; Djennaoui D; Zenati A; Claustres M; Roux AF
    Eur J Med Genet; 2009; 52(4):174-9. PubMed ID: 19375528
    [TBL] [Abstract][Full Text] [Related]  

  • 28. A deletion mutation in GJB6 cooperating with a GJB2 mutation in trans in non-syndromic deafness: A novel founder mutation in Ashkenazi Jews.
    Lerer I; Sagi M; Ben-Neriah Z; Wang T; Levi H; Abeliovich D
    Hum Mutat; 2001 Nov; 18(5):460. PubMed ID: 11668644
    [TBL] [Abstract][Full Text] [Related]  

  • 29. 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]  

  • 30. Compound heterozygosity for dominant and recessive GJB2 mutations: effect on phenotype and review of the literature.
    Welch KO; Marin RS; Pandya A; Arnos KS
    Am J Med Genet A; 2007 Jul; 143A(14):1567-73. PubMed ID: 17431919
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Exploring the clinical and epidemiological complexity of GJB2-linked deafness.
    Gualandi F; Ravani A; Berto A; Sensi A; Trabanelli C; Falciano F; Trevisi P; Mazzoli M; Tibiletti MG; Cristofari E; Burdo S; Ferlini A; Martini A; Calzolari E
    Am J Med Genet; 2002 Sep; 112(1):38-45. PubMed ID: 12239718
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Screening of families with autosomal recessive non-syndromic hearing impairment (ARNSHI) for mutations in GJB2 gene: Indian scenario.
    Maheshwari M; Vijaya R; Ghosh M; Shastri S; Kabra M; Menon PS
    Am J Med Genet A; 2003 Jul; 120A(2):180-4. PubMed ID: 12833397
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Cultural transmission of a sign language when deafness is caused by recessive alleles at two independent loci.
    Aoki K; Feldman MW
    Theor Popul Biol; 1994 Feb; 45(1):101-20. PubMed ID: 8023314
    [TBL] [Abstract][Full Text] [Related]  

  • 34. [An attempt to identify the most frequent genomic mutations responsible for isolated deafness in patients after cochlear implantation].
    Szyfter W; Pruszewicz A; Zenner HP; Pfister M; Szyfter K; Blin N; Wróbel M; Łaczkowska J; Gawlak A; Kupka S; Sekula A
    Otolaryngol Pol; 2001; 55(1):79-84. PubMed ID: 11355484
    [TBL] [Abstract][Full Text] [Related]  

  • 35. [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]  

  • 36. Deafness on the island of Providencia - Colombia: different etiology, different genetic counseling.
    Lattig MC; Gelvez N; Plaza SL; Tamayo G; Uribe JI; Salvatierra I; Bernal JE; Tamayo ML
    Genet Couns; 2008; 19(4):403-12. PubMed ID: 19239084
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Genotyping for Cx26 and Cx30 mutations in cases with congenital hearing loss.
    Evirgen N; Solak M; Dereköy S; Erdoğan M; Yildiz H; Eser B; Arikan S; Erkoç A
    Genet Test; 2008 Jun; 12(2):253-6. PubMed ID: 18554165
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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]  

  • 39. Spectrum of GJB2 (Cx26) gene mutations in Iranian Azeri patients with nonsyndromic autosomal recessive hearing loss.
    Davarnia B; Babanejad M; Fattahi Z; Nikzat N; Bazazzadegan N; Pirzade A; Farajollahi R; Nishimura C; Jalalvand K; Arzhangi S; Kahrizi K; Smith RJ; Najmabadi H
    Int J Pediatr Otorhinolaryngol; 2012 Feb; 76(2):268-71. PubMed ID: 22172221
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Ultrastructure of the hair in genetic prelingual deafness associated with the 35delG mutation in the connexin 26 gene (GJB2).
    Zhuravskiy SG; Kurus AA; Taraskina AE; Ivanov SA
    Bull Exp Biol Med; 2009 Jul; 148(1):79-81. PubMed ID: 19902103
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 7.