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Journal Abstract Search

166 related items for PubMed ID: 10424813

  • 1. 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
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  • 2. 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
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  • 3. 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 Mar; 47(8):395-9. PubMed ID: 12181639
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  • 4. Phenotypic characterization of a DFNA6 family showing progressive low-frequency sensorineural hearing impairment.
    Tóth T, Pfister M, Zenner HP, Sziklai I.
    Int J Pediatr Otorhinolaryngol; 2006 Feb; 70(2):201-6. PubMed ID: 16043233
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  • 5. Further evidence for linkage of low-mid frequency hearing impairment to the candidate region on chromosome 4p16.3.
    Brodwolf S, Böddeker IR, Ziegler A, Rausch P, Kunz J.
    Clin Genet; 2001 Aug; 60(2):155-60. PubMed ID: 11553051
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  • 6. 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
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  • 10. 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 18; 112(1):24-8. PubMed ID: 12483295
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  • 13. A second family with nonsyndromic sensorineural hearing loss linked to Xp21.2: refinement of the DFN4 locus within DMD.
    Pfister MH, Apaydin F, Turan O, Bereketoglu M, Bylgen V, Braendle U, Zenner HP, Lalwani AK.
    Genomics; 1998 Nov 01; 53(3):377-82. PubMed ID: 9799605
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  • 14. 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 01; 71(Pt 2):271-5. PubMed ID: 17166180
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  • 15. 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 01; 10(3):210-2. PubMed ID: 11973626
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  • 16. 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
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  • 18. 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 01; 20(5):621-6. PubMed ID: 10503584
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  • 19. Physical mapping of the mouse tilted locus identifies an association between human deafness loci DFNA6/14 and vestibular system development.
    Hurle B, Lane K, Kenney J, Tarantino LM, Bucan M, Brownstein BH, Ornitz DM.
    Genomics; 2001 Oct 01; 77(3):189-99. PubMed ID: 11597144
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