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Journal Abstract Search

161 related items for PubMed ID: 2320244

  • 1. 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; 40(4):671-6. PubMed ID: 2320244
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  • 2. Myotonic dystrophy is closely linked to the gene for muscle-type creatine kinase (CKMM).
    Brunner HG, Korneluk RG, Coerwinkel-Driessen M, MacKenzie A, Smeets H, Lambermon HM, van Oost BA, Wieringa B, Ropers HH.
    Hum Genet; 1989 Mar; 81(4):308-10. PubMed ID: 2703233
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  • 3. Tight linkage of creatine kinase (CKMM) to myotonic dystrophy on chromosome 19.
    Yamaoka LH, Pericak-Vance MA, Speer MC, Gaskell PC, Stajich J, Haynes C, Hung WY, Laberge C, Thibault MC, Mathieu J.
    Neurology; 1990 Feb; 40(2):222-6. PubMed ID: 2300239
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  • 4. 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; 34(3):189-94. PubMed ID: 2576756
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  • 5. Presymptomatic testing for myotonic dystrophy by means of the linked DNA marker APOC2.
    Haan EA, Mulley JC, Gedeon AK, Sheffield LJ, Sutherland GR.
    Med J Aust; 1988 Sep 19; 149(6):326-9. PubMed ID: 3047535
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  • 9. 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 Sep 19; 5(2):171-4. PubMed ID: 7917127
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  • 10. Linkage relationships of the apolipoprotein C1 gene and a cytochrome P450 gene (CYP2A) to myotonic dystrophy.
    Walsh KV, Harley HG, Brook JD, Rundle SA, Sarfarazi M, Harper PS, Shaw DJ.
    Hum Genet; 1990 Aug 19; 85(3):305-10. PubMed ID: 1975560
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  • 12. Assessment of a creatine kinase isoform M defect as a cause of myotonic dystrophy and the characterization of two novel CKMM polymorphisms.
    Bailly J, MacKenzie AE, Leblond S, Korneluk RG.
    Hum Genet; 1991 Mar 19; 86(5):457-62. PubMed ID: 2016086
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  • 13. Linkage analysis of the apolipoprotein C2 gene and myotonic dystrophy on human chromosome 19 reveals linkage disequilibrium in a French-Canadian population.
    MacKenzie AE, MacLeod HL, Hunter AG, Korneluk RG.
    Am J Hum Genet; 1989 Jan 19; 44(1):140-7. PubMed ID: 2562820
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  • 14. 3' creatine kinase (M-type) polymorphisms linked to myotonic dystrophy in Italian and Spanish populations.
    Gennarelli M, Novelli G, Cobo A, Baiget M, Dallapiccola B.
    Hum Genet; 1991 Oct 19; 87(6):654-6. PubMed ID: 1682233
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  • 15. Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy.
    Meredith AL, Huson SM, Lunt PW, Sarfarazi M, Harley HG, Brook JD, Shaw DJ, Harper PS.
    Br Med J (Clin Res Ed); 1986 Nov 22; 293(6558):1353-6. PubMed ID: 2878705
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  • 16. Direct haplotyping by double digestion of PCR-amplified creatine kinase (CKMM): application to myotonic dystrophy diagnosis.
    Lavedan C, Duros C, Savoy D, Leblond S, Bailly J, Korneluk R, Junien C.
    Genomics; 1990 Dec 22; 8(4):739-40. PubMed ID: 1980487
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  • 17. Linkage relationships of the insulin receptor gene with the complement component 3, LDL receptor, apolipoprotein C2 and myotonic dystrophy loci on chromosome 19.
    Shaw DJ, Meredith AL, Brook JD, Sarfarzi M, Harley HG, Huson SM, Bell GI, Harper PS.
    Hum Genet; 1986 Nov 22; 74(3):267-9. PubMed ID: 2877934
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  • 19. Myotonic dystrophy: molecular analysis of Israeli patients.
    Abeliovich D, Lerer I, Pashut-Lavon I, Cohen T.
    Biomed Pharmacother; 1994 Nov 22; 48(8-9):373-80. PubMed ID: 7858174
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