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PUBMED FOR HANDHELDS

Journal Abstract Search


128 related items for PubMed ID: 5173113

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  • 3. Charcot-Marie-Tooth disease with sensorineural hearing loss--an autosomal dominant trait.
    Kousseff BG, Hadro TA, Treiber DL, Wollner T, Morris C.
    Birth Defects Orig Artic Ser; 1982; 18(3B):223-8. PubMed ID: 7139106
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  • 10. Recessive inheritance in a neuronal motor neuropathy form of peroneal muscular atrophy.
    Frajman M, Brilla E, Gutiérrez A, Hun L.
    Rev Invest Clin; 1983; 35(4):305-8. PubMed ID: 6672928
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  • 12. Variation of phenotype in Charcot-Marie-Tooth disease.
    Baker RS, Upton AR.
    Neuropadiatrie; 1979 Aug; 10(3):290-5. PubMed ID: 583067
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  • 18. [Charcot-Marie-Tooth disease. Genetical, clinical and electrodiagnostic study of 2 families].
    Krstić S, Vidaković Z, Ignjatović M.
    Srp Arh Celok Lek; 1975 Sep; 103(9):769-77. PubMed ID: 1228922
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  • 19. Charcot-Marie-Tooth disease with Leber optic atrophy.
    McLeod JG, Low PA, Morgan JA.
    Neurology; 1978 Feb; 28(2):179-84. PubMed ID: 563998
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