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Journal Abstract Search

123 related items for PubMed ID: 6641396

  • 1. [Report of 9 cases of hereditary neuromuscular atrophy and investigation of its genetic patterns].
    Li ZX.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1983 Aug; 16(4):210-2. PubMed ID: 6641396
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  • 7. Recessively inherited Charcot-Marie-Tooth syndrome in identical twins.
    Beighton PH.
    Birth Defects Orig Artic Ser; 1971 Feb; 7(2):105. PubMed ID: 5173114
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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 Feb; 35(4):305-8. PubMed ID: 6672928
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  • 11. [Peroneal muscular atrophy associated with intellectual impairment and pyramidal signs].
    Sobue G, Ibi T, Matsuoka Y, Takahashi A.
    Rinsho Shinkeigaku; 1985 Jul; 25(7):818-25. PubMed ID: 4075646
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  • 15. [Hereditary motor and sensory neuropathy associated with retinitis pigmentosa and neural deafness].
    Murakami K, Sobue G, Takahashi A, Mitsuma T.
    Rinsho Shinkeigaku; 1986 Sep; 26(9):952-9. PubMed ID: 3791775
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  • 17. Controversy in genetic disorders.
    Sybert VP.
    Arch Dermatol; 1981 Jul; 117(7):380-1. PubMed ID: 6455091
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