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

180 related items for PubMed ID: 11313754

  • 1. 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; 9(3):165-70. PubMed ID: 11313754
    [Abstract] [Full Text] [Related]

  • 2. 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]

  • 3. 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]

  • 4. 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; 9(9):667-71. PubMed ID: 11571554
    [Abstract] [Full Text] [Related]

  • 5. A novel locus for autosomal dominant nonsyndromic hearing loss identified at 5q31.1-32 in a Chinese pedigree.
    Xia J, Deng H, Feng Y, Zhang H, Pan Q, Dai H, Long Z, Tang B, Deng H, Chen Y, Zhang R, Zheng D, He Y, Xia K.
    J Hum Genet; 2002 Sep; 47(12):635-40. PubMed ID: 12522684
    [Abstract] [Full Text] [Related]

  • 6. 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]

  • 7. Description of a large kindred with autosomal dominant inheritance of branchial arch anomalies, hearing loss, and ear pits, and exclusion of the branchio-oto-renal (BOR) syndrome gene locus (chromosome 8q13.3).
    Stratakis CA, Lin JP, Rennert OM.
    Am J Med Genet; 1998 Sep 23; 79(3):209-14. PubMed ID: 9788564
    [Abstract] [Full Text] [Related]

  • 8. 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 23; 8(12):991-3. PubMed ID: 11175289
    [Abstract] [Full Text] [Related]

  • 9. 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 23; 28(1):23-33. PubMed ID: 17694956
    [Abstract] [Full Text] [Related]

  • 10. Hearing impairment susceptibility in elderly men and the DFNA18 locus.
    Garringer HJ, Pankratz ND, Nichols WC, Reed T.
    Arch Otolaryngol Head Neck Surg; 2006 May 23; 132(5):506-10. PubMed ID: 16702566
    [Abstract] [Full Text] [Related]

  • 11. Evidence for linkage of restless legs syndrome to chromosome 9p: are there two distinct loci?
    Lohmann-Hedrich K, Neumann A, Kleensang A, Lohnau T, Muhle H, Djarmati A, König IR, Pramstaller PP, Schwinger E, Kramer PL, Ziegler A, Stephani U, Klein C.
    Neurology; 2008 Feb 26; 70(9):686-94. PubMed ID: 18032746
    [Abstract] [Full Text] [Related]

  • 12. [A study on localization of an autosomal dominant retinitis pigmentosa gene].
    Ma X, Wei R, Cai J, Zhu L.
    Zhonghua Yan Ke Za Zhi; 2002 Nov 26; 38(11):680-3. PubMed ID: 12487900
    [Abstract] [Full Text] [Related]

  • 13. 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 Nov 26; 6(6):548-51. PubMed ID: 9887371
    [Abstract] [Full Text] [Related]

  • 14. CORD9 a new locus for arCRD: mapping to 8p11, estimation of frequency, evaluation of a candidate gene.
    Danciger M, Hendrickson J, Lyon J, Toomes C, McHale JC, Fishman GA, Inglehearn CF, Jacobson SG, Farber DB.
    Invest Ophthalmol Vis Sci; 2001 Oct 26; 42(11):2458-65. PubMed ID: 11581183
    [Abstract] [Full Text] [Related]

  • 15. A novel locus for Usher syndrome type I, USH1G, maps to chromosome 17q24-25.
    Mustapha M, Chouery E, Torchard-Pagnez D, Nouaille S, Khrais A, Sayegh FN, Mégarbané A, Loiselet J, Lathrop M, Petit C, Weil D.
    Hum Genet; 2002 Apr 26; 110(4):348-50. PubMed ID: 11941484
    [Abstract] [Full Text] [Related]

  • 16. 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]

  • 17. DYT13, a novel primary torsion dystonia locus, maps to chromosome 1p36.13--36.32 in an Italian family with cranial-cervical or upper limb onset.
    Valente EM, Bentivoglio AR, Cassetta E, Dixon PH, Davis MB, Ferraris A, Ialongo T, Frontali M, Wood NW, Albanese A.
    Ann Neurol; 2001 Mar 05; 49(3):362-6. PubMed ID: 11261511
    [Abstract] [Full Text] [Related]

  • 18. Clinical description and genome wide linkage study of Y-sutural cataract and myopia in a Chinese family.
    Zhang Q, Guo X, Xiao X, Yi J, Jia X, Hejtmancik JF.
    Mol Vis; 2004 Nov 17; 10():890-900. PubMed ID: 15570218
    [Abstract] [Full Text] [Related]

  • 19. A novel locus for Usher syndrome type II, USH2B, maps to chromosome 3 at p23-24.2.
    Hmani M, Ghorbel A, Boulila-Elgaied A, Ben Zina Z, Kammoun W, Drira M, Chaabouni M, Petit C, Ayadi H.
    Eur J Hum Genet; 1999 Apr 17; 7(3):363-7. PubMed ID: 10234513
    [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 9.