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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

163 related items for PubMed ID: 10812644

  • 1.
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  • 2. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
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  • 3. Mutations in the COCH gene are a frequent cause of autosomal dominant progressive cochleo-vestibular dysfunction, but not of Meniere's disease.
    Usami S, Takahashi K, Yuge I, Ohtsuka A, Namba A, Abe S, Fransen E, Patthy L, Otting G, Van Camp G.
    Eur J Hum Genet; 2003 Oct; 11(10):744-8. PubMed ID: 14512963
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  • 4. Cracking the auditory genetic code: nonsyndromic hereditary hearing impairment.
    Lalwani AK, Castelein CM.
    Am J Otol; 1999 Jan; 20(1):115-32. PubMed ID: 9918184
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  • 7. Identification of five new mutations of PDS/SLC26A4 in Mediterranean families with hearing impairment.
    López-Bigas N, Melchionda S, de Cid R, Grifa A, Zelante L, Govea N, Arbonés ML, Gasparini P, Estivill X.
    Hum Mutat; 2001 Dec; 18(6):548. PubMed ID: 11748854
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  • 8. [Modern concepts of the role of heredity in the origin of monosymptomatic hearing disorders in children].
    Bliumina MG, Moskovkina AG.
    Vestn Otorinolaringol; 1980 Dec; (1):67-73. PubMed ID: 6990581
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  • 10. 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; 72(2):249-55. PubMed ID: 18022253
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  • 12. Genetic hearing loss.
    Keogh IJ, Godinho RN.
    Ir Med J; 2002 Jan; 95(1):5-7. PubMed ID: 11928792
    [No Abstract] [Full Text] [Related]

  • 13. Mouse models to study inner ear development and hereditary hearing loss.
    Friedman LM, Dror AA, Avraham KB.
    Int J Dev Biol; 2007 Jan; 51(6-7):609-31. PubMed ID: 17891721
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  • 15. Homozygosity mapping in a family presenting with schizophrenia, epilepsy and hearing impairment.
    Knight HM, Maclean A, Irfan M, Naeem F, Cass S, Pickard BS, Muir WJ, Blackwood DH, Ayub M.
    Eur J Hum Genet; 2008 Jun; 16(6):750-8. PubMed ID: 18322454
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  • 18. Mitochondrial deafness.
    Fischel-Ghodsian N.
    Ear Hear; 2003 Aug; 24(4):303-13. PubMed ID: 12923421
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  • 20. Genes responsible for human hereditary deafness: symphony of a thousand.
    Petit C.
    Nat Genet; 1996 Dec; 14(4):385-91. PubMed ID: 8944017
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