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Journal Abstract Search

126 related items for PubMed ID: 3118026

  • 1. An exclusion map for Von Recklinghausen neurofibromatosis.
    Sarfarazi M, Huson SM, Edwards JH.
    J Med Genet; 1987 Sep; 24(9):515-20. PubMed ID: 3118026
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  • 6. An exclusion map of Marfan syndrome.
    Blanton SH, Sarfarazi M, Eiberg H, de Groote J, Farndon PA, Kilpatrick MW, Child AH, Pope FM, Peltonen L, Francomano CA.
    J Med Genet; 1990 Feb; 27(2):73-7. PubMed ID: 2319588
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  • 11. Linkage analysis of von Recklinghausen neurofibromatosis to DNA markers on chromosome 17.
    Diehl SR, Boehnke M, Erickson RP, Baxter AB, Bruce MA, Lieberman JL, Platt DJ, Ploughman LM, Seiler KA, Sweet AM.
    Genomics; 1987 Dec; 1(4):361-3. PubMed ID: 2896631
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  • 13. Genetic linkage studies with neurofibromatosis: the question of heterogeneity.
    Spence MA, Sparkes RS, Parry DM, Bale SJ, Cortessis V, Mulvihill JJ.
    J Med Genet; 1987 Sep; 24(9):527-9. PubMed ID: 3118031
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  • 16. 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; 23(1):55-7. PubMed ID: 3081725
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  • 18. Chromosome 17 markers and von Recklinghausen neurofibromatosis: a genetic linkage study in a British population.
    Upadhyaya M, Sarfarazi M, Huson SM, Stephens K, Broadhead W, Harper PS.
    Genomics; 1987 Dec; 1(4):358-60. PubMed ID: 2896630
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  • 19. Genetic and physical map of the von Recklinghausen neurofibromatosis (NF1) region on chromosome 17.
    Yagle MK, Parruti G, Xu W, Ponder BA, Solomon E.
    Proc Natl Acad Sci U S A; 1990 Sep; 87(18):7255-9. PubMed ID: 2119504
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