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Journal Abstract Search

201 related items for PubMed ID: 2991117

  • 21. Presymptomatic detection and prenatal diagnosis for myotonic dystrophy by means of linked DNA markers.
    Norman AM, Floyd JL, Meredith AL, Harper PS.
    J Med Genet; 1989 Dec; 26(12):750-4. PubMed ID: 2575669
    [Abstract] [Full Text] [Related]

  • 22. The gene for apolipoprotein C-II is closely linked to the gene for apolipo-protein E on chromosome 19.
    Humphries SE, Berg K, Gill L, Cumming AM, Robertson FW, Stalenhoef AF, Williamson R, Børresen AL.
    Clin Genet; 1984 Nov; 26(5):389-96. PubMed ID: 6094053
    [Abstract] [Full Text] [Related]

  • 23. Myotonic dystrophy and gene mapping on human chromosome 19.
    Brook JD, Shaw DJ, Meredith AL.
    Biotechnol Genet Eng Rev; 1985 Nov; 3():311-47. PubMed ID: 3004536
    [No Abstract] [Full Text] [Related]

  • 24. A new polymorphic probe which defines the region of chromosome 19 containing the myotonic dystrophy locus.
    Johnson K, Shelbourne P, Davies J, Buxton J, Nimmo E, Siciliano MJ, Bachinski LL, Anvret M, Harley H, Rundle S.
    Am J Hum Genet; 1990 Jun; 46(6):1073-81. PubMed ID: 1971149
    [Abstract] [Full Text] [Related]

  • 25. Linkage relationships of the protein kinase C gamma gene which exclude it as a candidate for myotonic dystrophy.
    Johnson KJ, Jones PJ, Spurr N, Nimmo E, Davies J, Creed H, Weiss M, Williamson R.
    Cytogenet Cell Genet; 1988 Jun; 48(1):13-5. PubMed ID: 2460293
    [Abstract] [Full Text] [Related]

  • 26. The human ryanodine receptor gene: its mapping to 19q13.1, placement in a chromosome 19 linkage group, and exclusion as the gene causing myotonic dystrophy.
    MacKenzie AE, Korneluk RG, Zorzato F, Fujii J, Phillips M, Iles D, Wieringa B, Leblond S, Bailly J, Willard HF.
    Am J Hum Genet; 1990 Jun; 46(6):1082-9. PubMed ID: 1971150
    [Abstract] [Full Text] [Related]

  • 27. Gene mapping and myotonic dystrophy.
    Harper PS, Shaw D, Meredith L, Sarfarazi M, Brook D, Huson S.
    Prog Clin Biol Res; 1985 Jun; 177():61-76. PubMed ID: 2989839
    [No Abstract] [Full Text] [Related]

  • 28. Long-range restriction map of a region of human chromosome 19 containing the apolipoprotein genes, a CLL-associated translocation breakpoint, and two polymorphic MluI sites.
    Shaw DJ, Harley HG, Brook JD, McKeithan TW.
    Hum Genet; 1989 Aug; 83(1):71-4. PubMed ID: 2570021
    [Abstract] [Full Text] [Related]

  • 29. Localization of a human Na+,K+-ATPase alpha subunit gene to chromosome 19q12----q13.2 and linkage to the myotonic dystrophy locus.
    Harley HG, Brook JD, Jackson CL, Glaser T, Walsh KV, Sarfarazi M, Kent R, Lager M, Koch M, Harper PS.
    Genomics; 1988 Nov; 3(4):380-4. PubMed ID: 2907504
    [Abstract] [Full Text] [Related]

  • 30. Tight linkage between myotonic dystrophy and apolipoprotein E genes revealed with allele-specific oligonucleotides.
    Smeets B, Poddighe J, Brunner H, Ropers HH, Wieringa B.
    Hum Genet; 1988 Sep; 80(1):49-52. PubMed ID: 3417303
    [Abstract] [Full Text] [Related]

  • 31. Physical and genetic mapping of a novel chromosome 19 ERCC1 marker showing close linkage with myotonic dystrophy.
    Shutler G, MacKenzie AE, Brunner H, Wieringa B, de Jong P, Lohman FP, Leblond S, Bailly J, Korneluk RG.
    Genomics; 1991 Mar; 9(3):500-4. PubMed ID: 1674498
    [Abstract] [Full Text] [Related]

  • 32. The isolation of a genomic clone containing the apolipoprotein CII gene and the detection of linkage disequilibrium between two common DNA polymorphisms around the gene.
    Wallis SC, Donald JA, Forrest LA, Williamson R, Humphries SE.
    Hum Genet; 1984 Mar; 68(4):286-9. PubMed ID: 6096256
    [Abstract] [Full Text] [Related]

  • 33. RFLPs at the D19S19 locus of human chromosome 19 linked to myotonic dystrophy (DM).
    Roses AD, Pericak-Vance MA, Ross DA, Yamaoka L, Bartlett RJ.
    Nucleic Acids Res; 1986 Jul 11; 14(13):5569. PubMed ID: 3016653
    [No Abstract] [Full Text] [Related]

  • 34. Dimorphic markers for the human apolipoprotein CII gene locus.
    Frossard PM, Coleman RT, Funke H, Assmann G.
    Gene; 1987 Jul 11; 51(1):103-6. PubMed ID: 2885246
    [Abstract] [Full Text] [Related]

  • 35. Linkage analysis of peripheral neurofibromatosis (Von Recklinghausen disease) and chromosome 19 markers linked to myotonic dystrophy.
    Huson SM, Meredith AL, Sarfarazi M, Shaw DJ, Compston DA, Harper PS.
    J Med Genet; 1986 Feb 11; 23(1):55-7. PubMed ID: 3081725
    [Abstract] [Full Text] [Related]

  • 36. Exclusion of the C3 gene from the 19q133 to 19qter region by Southern analysis of human-rodent somatic cell hybrids, employing a cloned genomic C3 gene fragment.
    Wieacker P, Fey G, Voiculescu I, Ropers HH.
    Acta Anthropogenet; 1983 Feb 11; 7(2):107-12. PubMed ID: 6331467
    [Abstract] [Full Text] [Related]

  • 37. Localization of cloned unique DNA to three different regions of chromosome 19: screen for linkage probes for myotonic dystrophy.
    Yamaoka LH, Bartlett RJ, Ross DA, Fey GH, Ledbetter DH, Bruns G, Pericak-Vance MA, Herbstreith MH, Roses AD.
    J Neurogenet; 1985 Dec 11; 2(6):403-12. PubMed ID: 3001264
    [Abstract] [Full Text] [Related]

  • 38. 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 11; 40(2):222-6. PubMed ID: 2300239
    [Abstract] [Full Text] [Related]

  • 39. Usefulness of chromosome 19 RFLP haplotypes in the diagnosis of myotonic dystrophy.
    Nokelainen PT, Alanen-Kurki L, Somer HV, Pihko SH, Peltonen L.
    Muscle Nerve; 1991 May 11; 14(5):451-6. PubMed ID: 1678492
    [Abstract] [Full Text] [Related]

  • 40. A chromosome 19 clone from a translocation breakpoint shows close linkage and linkage disequilibrium with myotonic dystrophy.
    Korneluk RG, MacLeod HL, McKeithan TW, Brooks JD, MacKenzie AE.
    Genomics; 1989 Feb 11; 4(2):146-51. PubMed ID: 2567698
    [Abstract] [Full Text] [Related]

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