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

311 related items for PubMed ID: 17694956

  • 1. Linkage and association studies in a Malaysian family with autosomal recessive non-syndromic hearing loss.
    Farah WI, Aminuddin BS, Ruszymah BH.
    Malays J Pathol; 2006 Jun; 28(1):23-33. PubMed ID: 17694956
    [Abstract] [Full Text] [Related]

  • 2. Localization of a novel autosomal recessive non-syndromic hearing impairment locus DFNB63 to chromosome 11q13.3-q13.4.
    Tlili A, Masmoudi S, Dhouib H, Bouaziz S, Rebeh IB, Chouchen J, Turki K, Benzina Z, Charfedine I, Drira M, Ayadi H.
    Ann Hum Genet; 2007 Mar; 71(Pt 2):271-5. PubMed ID: 17166180
    [Abstract] [Full Text] [Related]

  • 3. Pendred syndrome (goitre and sensorineural hearing loss) maps to chromosome 7 in the region containing the nonsyndromic deafness gene DFNB4.
    Coyle B, Coffey R, Armour JA, Gausden E, Hochberg Z, Grossman A, Britton K, Pembrey M, Reardon W, Trembath R.
    Nat Genet; 1996 Apr; 12(4):421-3. PubMed ID: 8630497
    [Abstract] [Full Text] [Related]

  • 4. Mapping of a new autosomal recessive nonsyndromic hearing loss locus (DFNB32) to chromosome 1p13.3-22.1.
    Masmoudi S, Tlili A, Majava M, Ghorbel AM, Chardenoux S, Lemainque A, Zina ZB, Moala J, Männikkö M, Weil D, Lathrop M, Ala-Kokko L, Drira M, Petit C, Ayadi H.
    Eur J Hum Genet; 2003 Feb; 11(2):185-8. PubMed ID: 12634867
    [Abstract] [Full Text] [Related]

  • 5. A gene for autosomal dominant hearing impairment (DFNA14) maps to a region on chromosome 4p16.3 that does not overlap the DFNA6 locus.
    Van Camp G, Kunst H, Flothmann K, McGuirt W, Wauters J, Marres H, Verstreken M, Bespalova IN, Burmeister M, Van de Heyning PH, Smith RJ, Willems PJ, Cremers CW, Lesperance MM.
    J Med Genet; 1999 Jul; 36(7):532-6. PubMed ID: 10424813
    [Abstract] [Full Text] [Related]

  • 6. Hereditary postlingual sensorineural hearing loss mapping to chromosome Xq21.
    Manolis EN, Eavey RD, Sangwatanaroj S, Halpin C, Rosenbaum S, Watkins H, Jarcho J, Seidman CE, Seidman JG.
    Am J Otol; 1999 Sep; 20(5):621-6. PubMed ID: 10503584
    [Abstract] [Full Text] [Related]

  • 7. A novel locus for autosomal dominant nonsyndromic hearing loss (DFNA44) maps to chromosome 3q28-29.
    Modamio-Høybjør S, Moreno-Pelayo MA, Mencía A, del Castillo I, Chardenoux S, Armenta D, Lathrop M, Petit C, Moreno F.
    Hum Genet; 2003 Jan; 112(1):24-8. PubMed ID: 12483295
    [Abstract] [Full Text] [Related]

  • 8. A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36.
    Mustapha M, Chardenoux S, Nieder A, Salem N, Weissenbach J, el-Zir E, Loiselet J, Petit C.
    Eur J Hum Genet; 1998 Jan; 6(3):245-50. PubMed ID: 9781028
    [Abstract] [Full Text] [Related]

  • 9. DFNB31, a recessive form of sensorineural hearing loss, maps to chromosome 9q32-34.
    Mustapha M, Chouery E, Chardenoux S, Naboulsi M, Paronnaud J, Lemainque A, Mégarbané A, Loiselet J, Weil D, Lathrop M, Petit C.
    Eur J Hum Genet; 2002 Mar; 10(3):210-2. PubMed ID: 11973626
    [Abstract] [Full Text] [Related]

  • 10. A non-syndrome form of neurosensory, recessive deafness maps to the pericentromeric region of chromosome 13q.
    Guilford P, Ben Arab S, Blanchard S, Levilliers J, Weissenbach J, Belkahia A, Petit C.
    Nat Genet; 1994 Jan; 6(1):24-8. PubMed ID: 8136828
    [Abstract] [Full Text] [Related]

  • 11. Linkage of autosomal dominant hearing loss to the short arm of chromosome 1 in two families.
    Coucke P, Van Camp G, Djoyodiharjo B, Smith SD, Frants RR, Padberg GW, Darby JK, Huizing EH, Cremers CW, Kimberling WJ.
    N Engl J Med; 1994 Aug 18; 331(7):425-31. PubMed ID: 8035838
    [Abstract] [Full Text] [Related]

  • 12. A novel TECTA mutation confirms the recognizable phenotype among autosomal recessive hearing impairment families.
    Alasti F, Sanati MH, Behrouzifard AH, Sadeghi A, de Brouwer AP, Kremer H, Smith RJ, Van Camp G.
    Int J Pediatr Otorhinolaryngol; 2008 Feb 18; 72(2):249-55. PubMed ID: 18022253
    [Abstract] [Full Text] [Related]

  • 13. New gene for autosomal recessive non-syndromic hearing loss maps to either chromosome 3q or 19p.
    Chen A, Wayne S, Bell A, Ramesh A, Srisailapathy CR, Scott DA, Sheffield VC, Van Hauwe P, Zbar RI, Ashley J, Lovett M, Van Camp G, Smith RJ.
    Am J Med Genet; 1997 Sep 05; 71(4):467-71. PubMed ID: 9286457
    [Abstract] [Full Text] [Related]

  • 14. Identification of a locus on chromosome 7q31, DFNB14, responsible for prelingual sensorineural non-syndromic deafness.
    Mustapha M, Salem N, Weil D, el-Zir E, Loiselet J, Petit C.
    Eur J Hum Genet; 1998 Sep 05; 6(6):548-51. PubMed ID: 9887371
    [Abstract] [Full Text] [Related]

  • 15. DFNB40, a recessive form of sensorineural hearing loss, maps to chromosome 22q11.21-12.1.
    Delmaghani S, Aghaie A, Compain-Nouaille S, Ataie A, Lemainque A, Zeinali S, Lathrop M, Weil D, Petit C.
    Eur J Hum Genet; 2003 Oct 05; 11(10):816-8. PubMed ID: 14512974
    [Abstract] [Full Text] [Related]

  • 16. A new locus for late-onset, progressive, hereditary hearing loss DFNA20 maps to 17q25.
    Morell RJ, Friderici KH, Wei S, Elfenbein JL, Friedman TB, Fisher RA.
    Genomics; 2000 Jan 01; 63(1):1-6. PubMed ID: 10662538
    [Abstract] [Full Text] [Related]

  • 17. A new locus for autosomal recessive non-syndromal sensorineural hearing impairment (DFNB27) on chromosome 2q23-q31.
    Pulleyn LJ, Jackson AP, Roberts E, Carridice A, Muxworthy C, Houseman M, Al-Gazali LI, Lench NJ, Markham AF, Mueller RF.
    Eur J Hum Genet; 2000 Dec 01; 8(12):991-3. PubMed ID: 11175289
    [Abstract] [Full Text] [Related]

  • 18. Mapping of a new autosomal dominant nonsyndromic hearing loss locus (DFNA30) to chromosome 15q25-26.
    Mangino M, Flex E, Capon F, Sangiuolo F, Carraro E, Gualandi F, Mazzoli M, Martini A, Novelli G, Dallapiccola B.
    Eur J Hum Genet; 2001 Sep 01; 9(9):667-71. PubMed ID: 11571554
    [Abstract] [Full Text] [Related]

  • 19. A novel locus for autosomal dominant, non-syndromic hearing impairment (DFNA18) maps to chromosome 3q22 immediately adjacent to the DM2 locus.
    Bönsch D, Scheer P, Neumann C, Lang-Roth R, Seifert E, Storch P, Weiller C, Lamprecht-Dinnesen A, Deufel T.
    Eur J Hum Genet; 2001 Mar 01; 9(3):165-70. PubMed ID: 11313754
    [Abstract] [Full Text] [Related]

  • 20. Further evidence for a third deafness gene within the DFNA2 locus.
    Goldstein JA, Lalwani AK.
    Am J Med Genet; 2002 Apr 01; 108(4):304-9. PubMed ID: 11920835
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 16.