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Journal Abstract Search

48 related items for PubMed ID: 23926024

  • 1. [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]

  • 2. [Non-syndromic familial deafness. Review and genetic study].
    Guiral H, Flores JC, Risco J, Figuerola E, Pellicer F.
    Acta Otorrinolaringol Esp; 1996 Aug; 47(4):272-6. PubMed ID: 8962727
    [Abstract] [Full Text] [Related]

  • 3. [Hereditary spastic paraplegia with coordination disorders and sensorineural deafness].
    Badalian LO, Iadgarov IS, Temin PA, Arkhipov BA, Bulaeva NV.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1990 Aug; 90(9):94-7. PubMed ID: 2176054
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  • 4. Genotype-phenotype correlation for DFNA22: characterization of non-syndromic, autosomal dominant, progressive sensorineural hearing loss due to MYO6 mutations.
    Topsakal V, Hilgert N, van Dinther J, Tranebjaerg L, Rendtorff ND, Zarowski A, Offeciers E, Van Camp G, van de Heyning P.
    Audiol Neurootol; 2010 Aug; 15(4):211-20. PubMed ID: 19893302
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  • 6. [Etiological diagnosis of sensorineural deafness in children: a year-long review of genetic counseling for deaf people].
    Marlin S, Denoyelle F, Garabédian EN, Petit C.
    Ann Otolaryngol Chir Cervicofac; 1998 Feb; 115(1):3-8. PubMed ID: 9765703
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  • 8. A novel autosomal recessive non-syndromic deafness locus, DFNB66, maps to chromosome 6p21.2-22.3 in a large Tunisian consanguineous family.
    Tlili A, Männikkö M, Charfedine I, Lahmar I, Benzina Z, Ben Amor M, Driss N, Ala-Kokko L, Drira M, Masmoudi S, Ayadi H.
    Hum Hered; 2005 Feb; 60(3):123-8. PubMed ID: 16244493
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  • 10. 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
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  • 14. Familial deafness associated with iris degeneration and glaucoma.
    Rundle P, Lotery AJ, Archer DB, McGinnity FG.
    Eye (Lond); 1997 Jun; 11 ( Pt 4)():476-8. PubMed ID: 9425410
    [Abstract] [Full Text] [Related]

  • 15. Diffuse palmoplantar keratoderma with deafness.
    Hatamochi A, Nakagawa S, Ueki H, Miyoshi K, Iuchi I.
    Arch Dermatol; 1982 Aug; 118(8):605-7. PubMed ID: 6213205
    [Abstract] [Full Text] [Related]

  • 16. Familial gingival fibromatosis associated with progressive deafness in five generations of a family.
    Jones G, Wilroy RS, McHaney V.
    Birth Defects Orig Artic Ser; 1977 Aug; 13(3B):195-201. PubMed ID: 890092
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  • 17. [Gene mapping for autosomal dominant nonsyndromic hearing loss DFNA11].
    Yuan H, Han DY, Wang QJ, Zong L, Zhao YL.
    Zhonghua Er Bi Yan Hou Tou Jing Wai Ke Za Zhi; 2007 Jun; 42(6):422-7. PubMed ID: 17702415
    [Abstract] [Full Text] [Related]

  • 18. Mutations in the alternatively spliced exons of USH1C cause non-syndromic recessive deafness.
    Ouyang XM, Xia XJ, Verpy E, Du LL, Pandya A, Petit C, Balkany T, Nance WE, Liu XZ.
    Hum Genet; 2002 Jul; 111(1):26-30. PubMed ID: 12136232
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  • 19. Parental attitudes toward genetic testing for prelingual deafness in China.
    Fu S, Dong J, Wang C, Chen G.
    Int J Pediatr Otorhinolaryngol; 2010 Oct; 74(10):1122-5. PubMed ID: 20637511
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  • 20. Dominantly inherited low-frequency hearing loss.
    Arch Otolaryngol; 1968 Sep; 88(3):242-50. PubMed ID: 5663381
    [No Abstract] [Full Text] [Related]

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