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

168 related items for PubMed ID: 12123480

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

  • 2. Non-syndromic, autosomal-recessive deafness.
    Petersen MB, Willems PJ.
    Clin Genet; 2006 May; 69(5):371-92. PubMed ID: 16650073
    [Abstract] [Full Text] [Related]

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

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

  • 5. [Non-syndromic hereditary hearing impairment].
    Birkenhäger R, Aschendorff A, Schipper J, Laszig R.
    Laryngorhinootologie; 2007 Apr; 86(4):299-309; quiz 310-3. PubMed ID: 17407011
    [Abstract] [Full Text] [Related]

  • 6.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 7. Assessment of the genetic causes of recessive childhood non-syndromic deafness in the UK - implications for genetic testing.
    Hutchin T, Coy NN, Conlon H, Telford E, Bromelow K, Blaydon D, Taylor G, Coghill E, Brown S, Trembath R, Liu XZ, Bitner-Glindzicz M, Mueller R.
    Clin Genet; 2005 Dec; 68(6):506-12. PubMed ID: 16283880
    [Abstract] [Full Text] [Related]

  • 8.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 9. Deafness linked to DFNA2: one locus but how many genes?
    Van Hauwe P, Coucke PJ, Declau F, Kunst H, Ensink RJ, Marres HA, Cremers CW, Djelantik B, Smith SD, Kelley P, Van de Heyning PH, Van Camp G.
    Nat Genet; 1999 Mar; 21(3):263. PubMed ID: 10080176
    [No Abstract] [Full Text] [Related]

  • 10. Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.
    Coucke PJ, Van Hauwe P, Kelley PM, Kunst H, Schatteman I, Van Velzen D, Meyers J, Ensink RJ, Verstreken M, Declau F, Marres H, Kastury K, Bhasin S, McGuirt WT, Smith RJ, Cremers CW, Van de Heyning P, Willems PJ, Smith SD, Van Camp G.
    Hum Mol Genet; 1999 Jul; 8(7):1321-8. PubMed ID: 10369879
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 13. The role of connexins in human disease.
    Chang EH, Van Camp G, Smith RJ.
    Ear Hear; 2003 Aug; 24(4):314-23. PubMed ID: 12923422
    [Abstract] [Full Text] [Related]

  • 14. Deafness genes.
    Kitamura K, Takahashi K, Tamagawa Y, Noguchi Y, Kuroishikawa Y, Ishikawa K, Hagiwara H.
    J Med Dent Sci; 2000 Mar; 47(1):1-11. PubMed ID: 12162522
    [Abstract] [Full Text] [Related]

  • 15. Hereditary deafness and phenotyping in humans.
    Bitner-Glindzicz M.
    Br Med Bull; 2002 Mar; 63():73-94. PubMed ID: 12324385
    [Abstract] [Full Text] [Related]

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

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

  • 18. 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 Mar; 52(4):174-9. PubMed ID: 19375528
    [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 9.