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

404 related items for PubMed ID: 34194829

  • 1.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 2.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 3.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Diverse spectrum of rare deafness genes underlies early-childhood hearing loss in Japanese patients: a cross-sectional, multi-center next-generation sequencing study.
    Mutai H, Suzuki N, Shimizu A, Torii C, Namba K, Morimoto N, Kudoh J, Kaga K, Kosaki K, Matsunaga T.
    Orphanet J Rare Dis; 2013 Oct 28; 8():172. PubMed ID: 24164807
    [Abstract] [Full Text] [Related]

  • 6. Targeted next generation sequencing for molecular diagnosis of Usher syndrome.
    Aparisi MJ, Aller E, Fuster-García C, García-García G, Rodrigo R, Vázquez-Manrique RP, Blanco-Kelly F, Ayuso C, Roux AF, Jaijo T, Millán JM.
    Orphanet J Rare Dis; 2014 Nov 18; 9():168. PubMed ID: 25404053
    [Abstract] [Full Text] [Related]

  • 7. Compound heterozygous MYO7A mutations segregating Usher syndrome type 2 in a Han family.
    Zong L, Chen K, Wu X, Liu M, Jiang H.
    Int J Pediatr Otorhinolaryngol; 2016 Nov 18; 90():150-155. PubMed ID: 27729122
    [Abstract] [Full Text] [Related]

  • 8. PDZD7 and hearing loss: More than just a modifier.
    Booth KT, Azaiez H, Kahrizi K, Simpson AC, Tollefson WT, Sloan CM, Meyer NC, Babanejad M, Ardalani F, Arzhangi S, Schnieders MJ, Najmabadi H, Smith RJ.
    Am J Med Genet A; 2015 Dec 18; 167A(12):2957-65. PubMed ID: 26416264
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 11. Targeted next generation sequencing identified a novel mutation in MYO7A causing Usher syndrome type 1 in an Iranian consanguineous pedigree.
    Kooshavar D, Razipour M, Movasat M, Keramatipour M.
    Int J Pediatr Otorhinolaryngol; 2018 Jan 18; 104():10-13. PubMed ID: 29287847
    [Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 15. Novel compound heterozygous mutations in MYO7A gene associated with autosomal recessive sensorineural hearing loss in a Chinese family.
    Ma Y, Xiao Y, Zhang F, Han Y, Li J, Xu L, Bai X, Wang H.
    Int J Pediatr Otorhinolaryngol; 2016 Apr 18; 83():179-85. PubMed ID: 26968074
    [Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18. Molecular Analysis of Twelve Pakistani Families with Nonsyndromic or Syndromic Hearing Loss.
    Wang R, Han S, Khan A, Zhang X.
    Genet Test Mol Biomarkers; 2017 May 18; 21(5):316-321. PubMed ID: 28281779
    [Abstract] [Full Text] [Related]

  • 19.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 21.