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Journal Abstract Search

182 related items for PubMed ID: 7917127

  • 1. Prenatal diagnosis for the unstable CTG repeat sequence in myotonic dystrophy: a retrospective study in a French family.
    Lucotte G, Berriche S, David F, Mariotti M, Turpin JC.
    Genet Couns; 1994; 5(2):171-4. PubMed ID: 7917127
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  • 2. Prenatal diagnosis of congenital myotonic dystrophy and counseling of the pregnant mother: case report and literature review.
    Geifman-Holtzman O, Fay K.
    Am J Med Genet; 1998 Jul 07; 78(3):250-3. PubMed ID: 9677060
    [Abstract] [Full Text] [Related]

  • 3. Preclinical detection in Japanese families with myotonic dystrophy using polymorphic DNA markers.
    Takemoto Y, Miki T, Nakura J, Nishikawa K, Kamino K, Takeda S, Kuzu K, Osame M, Nakagawa M, Higuchi I.
    Jinrui Idengaku Zasshi; 1989 Sep 07; 34(3):189-94. PubMed ID: 2576756
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  • 4. Five years experience of predictive testing for myotonic dystrophy using linked DNA markers.
    Reardon W, Floyd JL, Myring J, Lazarou LP, Meredith AL, Harper PS.
    Am J Med Genet; 1992 Aug 01; 43(6):1006-11. PubMed ID: 1415325
    [Abstract] [Full Text] [Related]

  • 5. [Neonatal Steinert's disease: apropos of 2 cases in 2 successive generations].
    Bétrémieux P, Blin-Jezequel E, Lefrançois C, Le Marec B.
    J Genet Hum; 1985 Jan 01; 33(1):21-30. PubMed ID: 3856628
    [Abstract] [Full Text] [Related]

  • 6. Advances in myotonic dystrophy: a clinical and genetic perspective.
    Reardon W, Harper PS.
    Curr Opin Neurol Neurosurg; 1992 Oct 01; 5(5):605-9. PubMed ID: 1392133
    [Abstract] [Full Text] [Related]

  • 7. Presymptomatic and prenatal diagnosis in myotonic dystrophy by genetic linkage studies.
    Speer MC, Pericak-Vance MA, Yamaoka L, Hung WY, Ashley A, Stajich JM, Roses AD.
    Neurology; 1990 Apr 01; 40(4):671-6. PubMed ID: 2320244
    [Abstract] [Full Text] [Related]

  • 8. An intergenerational contraction of the CTG repeat in Japanese myotonic dystrophy.
    Matsumura R, Namikawa T, Miki T, Kihira T, Yamagata H, Mano Y, Takayanagi T.
    J Neurol Sci; 1996 Jul 01; 139(1):48-51. PubMed ID: 8836971
    [Abstract] [Full Text] [Related]

  • 9. Decrease in the size of the myotonic dystrophy CTG repeat during transmission from parent to child: implications for genetic counselling and genetic anticipation.
    Hunter AG, Jacob P, O'Hoy K, MacDonald I, Mettler G, Tsilfidis C, Korneluk RG.
    Am J Med Genet; 1993 Feb 01; 45(3):401-7. PubMed ID: 8434633
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  • 13. [Presymptomatic DNA diagnosis in Huntington chorea with linked DNA markers].
    Thies U, Schröder K, Bockel B, Zoll B, Lange H.
    Nervenarzt; 1991 Oct 01; 62(10):615-20. PubMed ID: 1684226
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  • 14. Clinical expression of myotonic dystrophy: the predictive role of DNA diagnosis.
    Can B, Schaefer FV, Malik S, Floyd M, Say B.
    J Okla State Med Assoc; 1998 Oct 01; 91(1):7-10. PubMed ID: 9503753
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  • 15. [Prenatal diagnosis of myotonic dystrophy: the first experience in Spain].
    Cobo AM, Martínez JM, Parra J, Pérez MM, Pradas J, Baiget M.
    Med Clin (Barc); 1990 Apr 14; 94(14):538-40. PubMed ID: 2355772
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  • 19. [Myotonic dystrophy of Steinert].
    Junien C.
    J Genet Hum; 1989 Jan 14; 37(1):51-4. PubMed ID: 2565953
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