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Journal Abstract Search

63 related items for PubMed ID: 6829114

  • 21. Variations in genetic assessment and recurrence risks quoted for childhood deafness: a survey of clinical geneticists.
    Parker MJ, Fortnum H, Young ID, Davis AC.
    J Med Genet; 1999 Feb; 36(2):125-30. PubMed ID: 10051011
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  • 24. [Genetic counseling in isolated deafness: apropos of 31 families].
    Larget-Piet L, Berthelot J, Larget-Piet A.
    J Genet Hum; 1976 Nov; 24 Suppl():189-93. PubMed ID: 1025269
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  • 26. A sensorineural progressive autosomal recessive form of isolated deafness, DFNB13, maps to chromosome 7q34-q36.
    Mustapha M, Chardenoux S, Nieder A, Salem N, Weissenbach J, el-Zir E, Loiselet J, Petit C.
    Eur J Hum Genet; 1998 Nov; 6(3):245-50. PubMed ID: 9781028
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  • 28. Autosomal dominant onychodystrophy and congenital sensorineural deafness.
    Kondoh T, Tsuru A, Matsumoto T, Matsuzaka T, Tsuji Y.
    J Hum Genet; 1999 Nov; 44(1):60-2. PubMed ID: 9929981
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  • 29. 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
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  • 30. Alport syndrome. Molecular genetic aspects.
    Hertz JM.
    Dan Med Bull; 2009 Aug; 56(3):105-52. PubMed ID: 19728970
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  • 31. Visual function in children with congenital sensorineural deafness.
    Siatkowski RM, Flynn JT, Hodges AV, Balkany TJ.
    Trans Am Ophthalmol Soc; 1993 Aug; 91():309-18; discussion 318-23. PubMed ID: 8140697
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  • 32. [Analysis of 104 children with hearing defects (author's transl)].
    Plöchl E, Tasser C.
    Padiatr Padol; 1980 Aug; 15(4):375-84. PubMed ID: 7193320
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  • 35. [Familial forms of deafness].
    Gapanovich VIa, Timoshenko PA, Gorbachuk VD, Kachan AA, Lipnitskaia LN.
    Vestn Otorinolaringol; 1972 Aug; 34(6):35-7. PubMed ID: 4665370
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  • 39. Genetic counselling for isolated hearing loss.
    Newton VE.
    J Laryngol Otol; 1989 Jan; 103(1):12-5. PubMed ID: 2921544
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