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Journal Abstract Search

156 related items for PubMed ID: 3081725

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  • 3. A genetic linkage study in 15 families of individuals with von Recklinghausen neurofibromatosis.
    Dunn BG, Ferrell RE, Riccardi VM.
    Am J Med Genet; 1985 Oct; 22(2):403-7. PubMed ID: 3931478
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  • 4. Coincidence of neurofibromatosis and myotonic dystrophy in a kindred.
    Ichikawa K, Crosley CJ, Culebras A, Weitkamp L.
    J Med Genet; 1981 Apr; 18(2):134-8. PubMed ID: 6787200
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  • 5. Linkage analysis of Von Recklinghausen neurofibromatosis: chromosomes 4 and 19.
    Dietz JN, Robbins T, Cannon LA, Schwartz CE, Carey JC, Johnson JP, Kivlin J, Skolnick MH.
    Genet Epidemiol; 1986 Apr; 3(5):313-21. PubMed ID: 3096816
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  • 6. Linkage analysis of neurofibromatosis (von Recklinghausen disease).
    Spence MA, Bader JL, Parry DM, Field LL, Funderburk SJ, Rubenstein AE, Gilman PA, Sparkes RS.
    J Med Genet; 1983 Oct; 20(5):334-7. PubMed ID: 6417334
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  • 8. Linkage analysis of myotonic dystrophy and sequences on chromosome 19 using a cloned complement 3 gene probe.
    Davies KE, Jackson J, Williamson R, Harper PS, Ball S, Sarfarazi M, Meredith L, Fey G.
    J Med Genet; 1983 Aug; 20(4):259-63. PubMed ID: 6620325
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  • 9. DNA linkage analysis in Von Recklinghausen neurofibromatosis.
    Seizinger BR, Rouleau G, Lane AH, Ozelius LJ, Faryniarz AG, Iannazzi J, Hobbs W, Roy JC, Falcone B, Huson S.
    J Med Genet; 1987 Sep; 24(9):529-30. PubMed ID: 3118032
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  • 12. Tight linkage of apolipoprotein C2 to myotonic dystrophy on chromosome 19.
    Pericak-Vance MA, Yamaoka LH, Assinder RI, Hung WY, Bartlett RJ, Stajich JM, Gaskell PC, Ross DA, Sherman S, Fey GH.
    Neurology; 1986 Nov; 36(11):1418-23. PubMed ID: 3762959
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  • 14. A refined genetic map of the region of chromosome 17 surrounding the von Recklinghausen neurofibromatosis (NF1) gene.
    Diehl SR, Boehnke M, Erickson RP, Ploughman LM, Seiler KA, Lieberman JL, Clarke HB, Bruce MA, Schorry EK, Pericak-Vance M.
    Am J Hum Genet; 1989 Jan; 44(1):33-7. PubMed ID: 2491779
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  • 15. Regional localisations and linkage relationships of seven RFLPs and myotonic dystrophy on chromosome 19.
    Shaw DJ, Meredith AL, Sarfarazi M, Harley HG, Huson SM, Brook JD, Bufton L, Litt M, Mohandas T, Harper PS.
    Hum Genet; 1986 Nov; 74(3):262-6. PubMed ID: 2877933
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  • 16. Von Recklinghausen neurofibromatosis: a linkage study of candidate and random marker genes.
    Ferrell RE, Buetow KH, Darby JK, Eichner JE, Murray JC, Smith R, Waziri M, Huson S, Riccardi VM.
    J Med Genet; 1987 Sep; 24(9):522-4. PubMed ID: 3118028
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  • 17. Genetic linkage between the loci for myotonic dystrophy and peptidase D.
    O'Brien T, Ball S, Sarfarazi M, Harper PS, Robson EB.
    Ann Hum Genet; 1983 May; 47(2):117-21. PubMed ID: 6881909
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  • 20. 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; 2(6):403-12. PubMed ID: 3001264
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