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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

357 related items for PubMed ID: 2989525

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  • 2. Genetic linkage between Becker muscular dystrophy and a polymorphic DNA sequence on the short arm of the X chromosome.
    Kingston HM, Thomas NS, Pearson PL, Sarfarazi M, Harper PS.
    J Med Genet; 1983 Aug; 20(4):255-8. PubMed ID: 6620324
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  • 7. Definitive localization of Becker muscular dystrophy in Xp by linkage to a cluster of DNA polymorphisms (DXS43 and DXS9).
    Fadda S, Mochi M, Roncuzzi L, Sangiorgi S, Sbarra D, Zatz M, Romeo G.
    Hum Genet; 1985 Aug; 71(1):33-6. PubMed ID: 2993155
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  • 9. Localisation of the Becker muscular dystrophy gene on the short arm of the X chromosome by linkage to cloned DNA sequences.
    Kingston HM, Sarfarazi M, Thomas NS, Harper PS.
    Hum Genet; 1984 Aug; 67(1):6-17. PubMed ID: 6086495
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  • 12. Mapping of X-linked Becker muscular dystrophy through crossovers identified by DNA polymorphisms and by haplotype characterization in somatic cell hybrids.
    Roncuzzi L, Fadda S, Mochi M, Prosperi L, Sangiorgi S, Santamaria R, Sbarra D, Besana D, Morandi L, Rocchi M.
    Am J Hum Genet; 1985 Mar; 37(2):407-17. PubMed ID: 2984927
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  • 13. DNA probe analysis for carrier detection and prenatal diagnosis of Duchenne muscular dystrophy: a standard diagnostic procedure.
    Bakker E, Bonten EJ, De Lange LF, Veenema H, Majoor-Krakauer D, Hofker MH, Van Ommen GJ, Pearson PL.
    J Med Genet; 1986 Dec; 23(6):573-80. PubMed ID: 2879929
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  • 17. A physical map of 4 million bp around the Duchenne muscular dystrophy gene on the human X-chromosome.
    van Ommen GJ, Verkerk JM, Hofker MH, Monaco AP, Kunkel LM, Ray P, Worton R, Wieringa B, Bakker E, Pearson PL.
    Cell; 1986 Nov 21; 47(4):499-504. PubMed ID: 2877741
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  • 18. The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophy.
    Harper PS, O'Brien T, Murray JM, Davies KE, Pearson P, Williamson R.
    J Med Genet; 1983 Aug 21; 20(4):252-4. PubMed ID: 6684693
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  • 19. Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy.
    Monaco AP, Bertelson CJ, Colletti-Feener C, Kunkel LM.
    Hum Genet; 1987 Mar 21; 75(3):221-7. PubMed ID: 2881877
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