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Journal Abstract Search

130 related items for PubMed ID: 7203475

  • 21. Charcot-Marie-Tooth disease in northern Sweden: pedigree analysis and the presence of the duplication in chromosome 17p11.2.
    Holmberg BH, Holmgren G, Nelis E, van Broeckhoven C, Westerberg B.
    J Med Genet; 1994 Jun; 31(6):435-41. PubMed ID: 8071969
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  • 22. Clinical and molecular studies in a family with probable X-linked dominant Charcot-Marie-Tooth disease involving the central nervous system.
    Hisama FM, Lee HH, Vashlishan A, Tekumalla P, Russell DS, Auld E, Goldstein JM.
    Arch Neurol; 2001 Nov; 58(11):1891-6. PubMed ID: 11709000
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  • 23. Genetic aspects of hereditary motor and sensory neuropathy (types I and II).
    Harding AE, Thomas PK.
    J Med Genet; 1980 Oct; 17(5):329-36. PubMed ID: 7218272
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  • 24. Intermediate nerve conduction velocities define X-linked Charcot-Marie-Tooth neuropathy families.
    Nicholson G, Nash J.
    Neurology; 1993 Dec; 43(12):2558-64. PubMed ID: 8255457
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  • 25. Charcot-Marie-Tooth disease with sex-linked inheritance, linkage studies and abnormal serum alkaline phosphatase levels.
    de Weerdt CJ.
    Eur Neurol; 1978 Dec; 17(6):336-44. PubMed ID: 744199
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  • 28. [X-linked recessively inherited peroneal muscular atrophy].
    Wang DS.
    Zhonghua Shen Jing Jing Shen Ke Za Zhi; 1989 Jun; 22(3):139-40, 190. PubMed ID: 2591266
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  • 32. [Relationships between genotype and phenotype in Charcot-Marie-Tooth disease].
    Câmpeanu E, Morariu M.
    Rev Roum Neurol; 1970 Jun; 7(1):47-56. PubMed ID: 5527990
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  • 34. Charcot-Marie-Tooth disease in northern Sweden: an epidemiological and clinical study.
    Holmberg BH.
    Acta Neurol Scand; 1993 May; 87(5):416-22. PubMed ID: 8333247
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