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

253 related items for PubMed ID: 12707188

  • 1. Progression of low-frequency sensorineural hearing loss (DFNA6/14-WFS1).
    Pennings RJ, Bom SJ, Cryns K, Flothmann K, Huygen PL, Kremer H, Van Camp G, Cremers CW.
    Arch Otolaryngol Head Neck Surg; 2003 Apr; 129(4):421-6. PubMed ID: 12707188
    [Abstract] [Full Text] [Related]

  • 2. Audiometric characteristics of a Dutch family linked to DFNA15 with a novel mutation (p.L289F) in POU4F3.
    Pauw RJ, van Drunen FJ, Collin RW, Huygen PL, Kremer H, Cremers CW.
    Arch Otolaryngol Head Neck Surg; 2008 Mar; 134(3):294-300. PubMed ID: 18347256
    [Abstract] [Full Text] [Related]

  • 3. A Dutch family with hearing loss linked to the DFNA20/26 locus: longitudinal analysis of hearing impairment.
    Kemperman MH, De Leenheer EM, Huygen PL, van Wijk E, van Duijnhoven G, Cremers FP, Kremer H, Cremers CW.
    Arch Otolaryngol Head Neck Surg; 2004 Mar; 130(3):281-8. PubMed ID: 15023833
    [Abstract] [Full Text] [Related]

  • 4. Variable degrees of hearing impairment in a Dutch DFNX4 (DFN6) family.
    Weegerink NJ, Huygen PL, Schraders M, Kremer H, Pennings RJ, Kunst HP.
    Hear Res; 2011 Dec; 282(1-2):167-77. PubMed ID: 21893181
    [Abstract] [Full Text] [Related]

  • 5.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 7.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

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

  • 9. [From gene to disease; non-syndromic, autosomal dominant, low-frequency sensorineural hearing loss (DFNA6/14)].
    Pennings RJ, Cryns K, Huygen PL, van Camp G, Cremers CW.
    Ned Tijdschr Geneeskd; 2003 Nov 01; 147(44):2170-2. PubMed ID: 14626834
    [Abstract] [Full Text] [Related]

  • 10. A new autosomal-dominant locus (DFNA12) is responsible for a nonsyndromic, midfrequency, prelingual and nonprogressive sensorineural hearing loss.
    Govaerts PJ, De Ceulaer G, Daemers K, Verhoeven K, Van Camp G, Schatteman I, Verstreken M, Willems PJ, Somers T, Offeciers FE.
    Am J Otol; 1998 Nov 01; 19(6):718-23. PubMed ID: 9831143
    [Abstract] [Full Text] [Related]

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

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

  • 13. Autosomal dominant low-frequency hearing impairment (DFNA6/14): a clinical and genetic family study.
    Bom SJ, Van Camp G, Cryns K, Admiraal RJ, Huygen PL, Cremers CW.
    Otol Neurotol; 2002 Nov 01; 23(6):876-84. PubMed ID: 12438850
    [Abstract] [Full Text] [Related]

  • 14. Confirmation of genetic homogeneity of nonsyndromic low-frequency sensorineural hearing loss by linkage analysis and a DFNA6/14 mutation in a Japanese family.
    Komatsu K, Nakamura N, Ghadami M, Matsumoto N, Kishino T, Ohta T, Niikawa N, Yoshiura K.
    J Hum Genet; 2002 Nov 01; 47(8):395-9. PubMed ID: 12181639
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16. Hearing loss in the nonocular Stickler syndrome caused by a COL11A2 mutation.
    Admiraal RJ, Brunner HG, Dijkstra TL, Huygen PL, Cremers CW.
    Laryngoscope; 2000 Mar 01; 110(3 Pt 1):457-61. PubMed ID: 10718438
    [Abstract] [Full Text] [Related]

  • 17. Pure tone hearing thresholds and speech recognition scores in Dutch patients carrying mutations in the USH2A gene.
    Pennings RJ, Huygen PL, Weston MD, van Aarem A, Wagenaar M, Kimberling WJ, Cremers CW.
    Otol Neurotol; 2003 Jan 01; 24(1):58-63. PubMed ID: 12544030
    [Abstract] [Full Text] [Related]

  • 18. Phenotypic characterization of hereditary hearing impairment linked to DFNA25.
    Thirlwall AS, Brown DJ, McMillan PM, Barker SE, Lesperance MM.
    Arch Otolaryngol Head Neck Surg; 2003 Aug 01; 129(8):830-5. PubMed ID: 12925340
    [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 13.