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Journal Abstract Search

277 related items for PubMed ID: 569219

  • 1. Charcot-Marie-Tooth disease and schizophrenia in identical twins.
    Manyam NV, Cowell HR, Katz L.
    JAMA; 1979 Jan 05; 241(1):54-5. PubMed ID: 569219
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  • 2. [Polymorphism of Charcot-Marie-Tooth neural amyotrophy in uniovular twins].
    Popov'ian MD, Dubinskaia EE, Ageeva TS.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1977 Jan 05; 77(10):1446-8. PubMed ID: 563155
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  • 4. [A case of Charcot-Marie-Tooth muscular atrophy in monozygotic twins].
    Mrowiec W, Termińska-Mrowiec K.
    Wiad Lek; 1987 Sep 15; 40(18):1292-5. PubMed ID: 3445607
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  • 7. Autosomal recessive inheritance of Charcot-Marie-Tooth disease associated with sensorineural deafness.
    Cornell J, Sellars S, Beighton P.
    Clin Genet; 1984 Feb 15; 25(2):163-5. PubMed ID: 6705250
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  • 8. Peroneal musclar atrophy (of Charcot-Marie-Tooth) in two African brothers.
    Billinghurst JR.
    Afr J Med Med Sci; 1976 Dec 15; 5(4):269-72. PubMed ID: 829740
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  • 13. Variation of phenotype in Charcot-Marie-Tooth disease.
    Baker RS, Upton AR.
    Neuropadiatrie; 1979 Aug 15; 10(3):290-5. PubMed ID: 583067
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  • 14. A family with Charcot-Marie-Tooth's disease, showing a probable X-linked incompletely dominant inheritance.
    Iselius L, Grimby L.
    Hereditas; 1982 Aug 15; 97(1):157-8. PubMed ID: 6890052
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  • 18. Naevoid basal cell carcinoma syndrome and Charcot-Marie-Tooth disease: two autosomal dominant disorders segregating in a family.
    Heimler A, Friedman E, Rosenthal AD.
    J Med Genet; 1978 Aug 15; 15(4):288-91. PubMed ID: 712760
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  • 20. Recessive inheritance in a neuronal motor neuropathy form of peroneal muscular atrophy.
    Frajman M, Brilla E, Gutiérrez A, Hun L.
    Rev Invest Clin; 1983 Aug 15; 35(4):305-8. PubMed ID: 6672928
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