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PUBMED FOR HANDHELDS

Journal Abstract Search


91 related items for PubMed ID: 1264090

  • 21.
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  • 23. [Roussy-Levy hereditary areflexic dysstasia. Its historical relation to Friedreich's disease, Charcot-Marie-Tooth atrophy and Dejerine-Sottas hypertrophic neuritis; the present status of the original family; the nosologic role of this entity].
    Lapresle J.
    Rev Neurol (Paris); 1982; 138(12):967-78. PubMed ID: 6763298
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  • 24.
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  • 26. [Tricho-rhino-phalangeal syndrome with autosomal dominant inheritance (author's transl)].
    Frisch H, Vormittag W.
    Z Kinderheilkd; 1975 Aug 11; 120(2):141-50. PubMed ID: 1163078
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  • 28. [Dermatologlyphic investigations in a kindred manifesting familial atrial septal defect (ostium secundum). A contribution to the problem of genetic counselling in multifactorial inheritance (author's transl)].
    Vormittag W, Ferlitsch A.
    Wien Klin Wochenschr; 1975 Feb 07; 87(3):99-101. PubMed ID: 1136515
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  • 31. [Autosomal-dominant motor-sensory neuropathy type I: intrafamilial polymorphism in the Roussy-Lévy syndrome].
    Badalian LO, Temin PA, Arkhipov BA, Avakian GN, Zavedenko NN.
    Zh Nevropatol Psikhiatr Im S S Korsakova; 1988 Feb 07; 88(11):45-9. PubMed ID: 3223157
    [Abstract] [Full Text] [Related]

  • 32. A kinship with the Roussy-Levy syndrome.
    Yudell A, Dyck PJ, Lambert EH.
    Arch Neurol; 1965 Oct 07; 13(4):432-40. PubMed ID: 5834704
    [No Abstract] [Full Text] [Related]

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  • 36. [Diagnostic problems in mosaic-Downs-syndrome (author's transl)].
    Zankl H, Rodewald A.
    Klin Padiatr; 1977 Nov 07; 189(6):430-9. PubMed ID: 146109
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  • 37. [Dejerine-Roussy syndrome (author's transl)].
    Kameyama M.
    No Shinkei Geka; 1976 Nov 07; 4(11):1045-9. PubMed ID: 1034225
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  • 38. [Discrimination of Down's syndrome with dermatoglyphic examination: an application of two dimensional graphic representation (author's transl)].
    Kimura S.
    Jinrui Idengaku Zasshi; 1978 Mar 07; 23(1):39-58. PubMed ID: 149871
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