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Journal Abstract Search

215 related items for PubMed ID: 8962727

  • 21. 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]

  • 22. Unexpected genetic heterogeneity in a large consanguineous Brazilian pedigree presenting deafness.
    Lezirovitz K, Pardono E, de Mello Auricchio MT, de Carvalho E Silva FL, Lopes JJ, Abreu-Silva RS, Romanos J, Batissoco AC, Mingroni-Netto RC.
    Eur J Hum Genet; 2008 Jan; 16(1):89-96. PubMed ID: 17851452
    [Abstract] [Full Text] [Related]

  • 23. Genetic heterogeneity study of non-syndromic autosomal recessive sensorineural deafness within the Tunisian population.
    Chaabani H, Ben Arab S, Chebbi K.
    Ann Genet; 1995 Jan; 38(3):158-61. PubMed ID: 8540687
    [Abstract] [Full Text] [Related]

  • 24. Etiological diagnosis of bilateral, sensorineural hearing impairment in a pediatric Greek population.
    Riga M, Psarommatis I, Lyra Ch, Douniadakis D, Tsakanikos M, Neou P, Apostolopoulos N.
    Int J Pediatr Otorhinolaryngol; 2005 Apr; 69(4):449-55. PubMed ID: 15763280
    [Abstract] [Full Text] [Related]

  • 25. Recurrence risks for near relatives of children with sensori-neural deafness.
    Koehn D, Morgan K, Fraser FC.
    Genet Couns; 1990 Apr; 1(2):127-32. PubMed ID: 2080997
    [Abstract] [Full Text] [Related]

  • 26. [Norrie-Wardburg syndrome].
    Skevas A, Kastanioudakis I, Daniilidis B, Exarchakos G.
    Laryngorhinootologie; 1992 Oct; 71(10):534-6. PubMed ID: 1418232
    [Abstract] [Full Text] [Related]

  • 27. Clinical and genetic heterogeneity in X-linked deafness.
    Reardon W, Middleton-Price HR, Malcolm S, Phelps P, Bellman S, Luxon L, Martin JA, Bumby A, Pembrey ME.
    Br J Audiol; 1992 Apr; 26(2):109-14. PubMed ID: 1628115
    [Abstract] [Full Text] [Related]

  • 28. Otospongiosis as a genetic disease. Early detection, medical management, and prevention.
    Causse JR, Causse JB.
    Am J Otol; 1984 Jan; 5(3):211-23. PubMed ID: 6372501
    [Abstract] [Full Text] [Related]

  • 29. A novel locus for non-syndromic sensorineural deafness (DFN6) maps to chromosome Xp22.
    del Castillo I, Villamar M, Sarduy M, Romero L, Herraiz C, Hernández FJ, Rodríguez M, Borrás I, Montero A, Bellón J, Tapia MC, Moreno F.
    Hum Mol Genet; 1996 Sep; 5(9):1383-7. PubMed ID: 8872482
    [Abstract] [Full Text] [Related]

  • 30. [Clinical study of a single congenital stapes malformation with possible X-linked dominant inheritance].
    Zhang G, Sun L, Wang X, Wang H, Zhang B, Jin H, Wang H.
    Lin Chuang Er Bi Yan Hou Ke Za Zhi; 2005 Aug; 19(16):745-7. PubMed ID: 16320716
    [Abstract] [Full Text] [Related]

  • 31. [Non-syndromic autosomal dominant type deafness: report of a family with 26 cases].
    Liu JZ, Cheng HB, Yang N, Lin LQ, Xu QY, Gu X, Shi YC, Yang SM, Shen LY, Song D, Wang T, Wang W, Li Q, Li H.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Aug; 30(4):501. PubMed ID: 23926024
    [No Abstract] [Full Text] [Related]

  • 32. [Genetics of congenital deafness].
    Faundes V, Pardo RA, Castillo Taucher S.
    Med Clin (Barc); 2012 Oct 20; 139(10):446-51. PubMed ID: 22538062
    [Abstract] [Full Text] [Related]

  • 33. X-linked inheritance of ocular albinism with late-onset sensorineural deafness.
    Winship I, Gericke G, Beighton P.
    Am J Med Genet; 1984 Dec 20; 19(4):797-803. PubMed ID: 6542750
    [Abstract] [Full Text] [Related]

  • 34. [Hereditary deafness in Kirov oblast: a genetic epidemiological study].
    Zinchenko RA, Osetrova AA, Sharonova EI, El'chinova GI.
    Genetika; 2012 Mar 20; 48(3):381-8. PubMed ID: 22679785
    [Abstract] [Full Text] [Related]

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  • 37. Nonsyndromal profound genetic deafness in childhood.
    Cremers CW, Marres HA, van Rijn PM.
    Ann N Y Acad Sci; 1991 Mar 20; 630():191-6. PubMed ID: 1952589
    [Abstract] [Full Text] [Related]

  • 38. Nonsyndromic deafness.
    Nance WE.
    Birth Defects Orig Artic Ser; 1980 Mar 20; 16(7):35-46. PubMed ID: 7011439
    [No Abstract] [Full Text] [Related]

  • 39. Genetic hearing impairment in the Dalmatian dog. An audiometric, genetic and morphologic study in 53 dogs.
    Anderson H, Henricson B, Lundquist PG, Wedenberg E, Wersäll J.
    Acta Otolaryngol; 1968 Mar 20; ():Suppl 232:1-34. PubMed ID: 5655384
    [No Abstract] [Full Text] [Related]

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