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.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

349 related items for PubMed ID: 26561413

  • 21.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 22.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 23.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 24.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 25.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 26.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 27.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 28. Spectrum and frequencies of non GJB2 gene mutations in Czech patients with early non-syndromic hearing loss detected by gene panel NGS and whole-exome sequencing.
    Safka Brozkova D, Poisson Marková S, Mészárosová AU, Jenčík J, Čejnová V, Čada Z, Laštůvková J, Rašková D, Seeman P.
    Clin Genet; 2020 Dec; 98(6):548-554. PubMed ID: 32860223
    [Abstract] [Full Text] [Related]

  • 29. Identification of novel variants in Iranian consanguineous pedigrees with nonsyndromic hearing loss by next-generation sequencing.
    Bitarafan F, Seyedena SY, Mahmoudi M, Garshasbi M.
    J Clin Lab Anal; 2020 Dec; 34(12):e23544. PubMed ID: 32864763
    [Abstract] [Full Text] [Related]

  • 30. Screening for MYO15A gene mutations in autosomal recessive nonsyndromic, GJB2 negative Iranian deaf population.
    Fattahi Z, Shearer AE, Babanejad M, Bazazzadegan N, Almadani SN, Nikzat N, Jalalvand K, Arzhangi S, Esteghamat F, Abtahi R, Azadeh B, Smith RJ, Kahrizi K, Najmabadi H.
    Am J Med Genet A; 2012 Aug; 158A(8):1857-64. PubMed ID: 22736430
    [Abstract] [Full Text] [Related]

  • 31. Detection of the 35delG/GJB2 and del(GJB6-D13S1830) mutations in Venezuelan patients with autosomal recessive nonsyndromic hearing loss.
    Utrera R, Ridaura V, Rodríguez Y, Rojas MJ, Mago L, Angeli S, Henríquez O.
    Genet Test; 2007 Aug; 11(4):347-52. PubMed ID: 18294049
    [Abstract] [Full Text] [Related]

  • 32.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 33.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 34. Whole exome sequencing of six Chinese families with hereditary non-syndromic hearing loss.
    Liang P, Chen F, Wang S, Li Q, Li W, Wang J, Chen J, Zha D.
    Int J Pediatr Otorhinolaryngol; 2021 Sep; 148():110817. PubMed ID: 34265623
    [Abstract] [Full Text] [Related]

  • 35. Genetic etiology study of the non-syndromic deafness in Chinese Hans by targeted next-generation sequencing.
    Yang T, Wei X, Chai Y, Li L, Wu H.
    Orphanet J Rare Dis; 2013 Jun 14; 8():85. PubMed ID: 23767834
    [Abstract] [Full Text] [Related]

  • 36.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 37. Prevalence of GJB2 Mutations in Affected Individuals from United Arab Emirates with Autosomal Recessive Nonsyndromic Hearing Loss.
    Tlili A, Al Mutery A, Kamal Eddine Ahmad Mohamed W, Mahfood M, Hadj Kacem H.
    Genet Test Mol Biomarkers; 2017 Nov 14; 21(11):686-691. PubMed ID: 29016196
    [Abstract] [Full Text] [Related]

  • 38. GJB2 mutations in Turkish patients with ARNSHL: prevalence and two novel mutations.
    Kalay E, Caylan R, Kremer H, de Brouwer AP, Karaguzel A.
    Hear Res; 2005 May 14; 203(1-2):88-93. PubMed ID: 15855033
    [Abstract] [Full Text] [Related]

  • 39.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 40. A novel mutation in the TMC1 gene causes non-syndromic hearing loss in a Moroccan family.
    Bakhchane A, Charoute H, Nahili H, Roky R, Rouba H, Charif M, Lenaers G, Barakat A.
    Gene; 2015 Dec 10; 574(1):28-33. PubMed ID: 26226225
    [Abstract] [Full Text] [Related]

    Page: [Previous] [Next] [New Search]
    of 18.