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PUBMED FOR HANDHELDS

Journal Abstract Search

157 related items for PubMed ID: 2912889

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  • 6. Deletion screening and prenatal diagnosis of Duchenne muscular dystrophy using cDNA probes Cf 23a and Cf 56a.
    Herrmann FH, Wulff K, Schütz M, Wehnert M.
    Eur J Pediatr; 1990 Jan; 149(4):263-5. PubMed ID: 1968008
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  • 7. Direct carrier detection by in situ suppression hybridization with cosmid clones of the Duchenne/Becker muscular dystrophy locus.
    Ried T, Mahler V, Vogt P, Blonden L, van Ommen GJ, Cremer T, Cremer M.
    Hum Genet; 1990 Oct; 85(6):581-6. PubMed ID: 2227948
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  • 8. Possibilities and limitation of prenatal diagnosis and carrier determination for Duchenne and Becker muscular dystrophy using cDNA probes.
    Speer A, Spiegler AW, Hanke R, Grade K, Giertler U, Schieck J, Forrest S, Davies KE, Neumann R, Bollmann R.
    J Med Genet; 1989 Jan; 26(1):1-5. PubMed ID: 2918522
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  • 9. Duchenne muscular dystrophy in Wales: impact of DNA linkage analysis and cDNA deletion screening.
    Norman AM, Upadhyaya M, Thomas NS, Roberts K, Harper PS.
    J Med Genet; 1989 Sep; 26(9):565-71. PubMed ID: 2810340
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  • 10. [Molecular biology in diagnosis and detection of deletion in Duchenne muscular dystrophy].
    Graninger W, Wintersberger W, Meron G, Smolen J, Toifl K, Vormittag W.
    Wien Klin Wochenschr; 1991 Sep; 103(7):207-9. PubMed ID: 2063586
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  • 11. Carrier diagnosis of Duchenne muscular dystrophy using restriction fragment length polymorphisms.
    Hejtmancik JF, Harris SG, Tsao CC, Ward PA, Caskey CT.
    Neurology; 1986 Dec; 36(12):1553-62. PubMed ID: 2878392
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  • 12. Molecular-genetic study of Duchenne and Becker muscular dystrophies: deletion analyses of 45 Japanese patients and segregation analyses in their families with RFLPs based on the data from normal Japanese females.
    Sugino S, Fujishita S, Kamimura N, Matsumoto T, Wapenaar MC, Deng HX, Shibuya N, Miike T, Niikawa N.
    Am J Med Genet; 1989 Dec; 34(4):555-61. PubMed ID: 2576185
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  • 13. Deletion screening in patients with Duchenne muscular dystrophy.
    Wulff K, Herrmann FH, Wapenaar MC, Wehnert M.
    J Neurol; 1989 Dec; 236(8):470-3. PubMed ID: 2614492
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  • 14. The use of field-inversion gel electrophoresis for deletion detection in Duchenne muscular dystrophy.
    Chen JD, Denton MJ, Morgan G, Pearn JH, Mackinlay AG.
    Am J Hum Genet; 1988 May; 42(5):777-80. PubMed ID: 3358426
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  • 15. Duchenne muscular dystrophy: high frequency of deletions.
    Bartlett RJ, Pericak-Vance MA, Koh J, Yamaoka LH, Chen JC, Hung WY, Speer MC, Wapenaar MC, Van Ommen GJ, Bakker E.
    Neurology; 1988 Jan; 38(1):1-4. PubMed ID: 3275902
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  • 16. Prenatal diagnosis of Duchenne muscular dystrophy: prospective linkage analysis and retrospective dystrophin cDNA analysis.
    Ward PA, Hejtmancik JF, Witkowski JA, Baumbach LL, Gunnell S, Speer J, Hawley P, Tantravahi U, Caskey CT.
    Am J Hum Genet; 1989 Feb; 44(2):270-81. PubMed ID: 2643315
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  • 17. High frequency of de novo deletions in Mexican Duchenne and Becker muscular dystrophy patients. Implications for genetic counseling.
    Alcántara MA, Villarreal MT, Del Castillo V, Gutiérrez G, Saldaña Y, Maulen I, Lee R, Macías M, Orozco L.
    Clin Genet; 1999 May; 55(5):376-80. PubMed ID: 10422811
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  • 18. Molecular deletion analysis in Duchenne muscular dystrophy.
    Thomas NS, Ray PN, Worton RG, Harper PS.
    J Med Genet; 1986 Dec; 23(6):509-15. PubMed ID: 2879923
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  • 19. Increased chloride efflux in fibroblasts from X-linked muscular dystrophies and clones from Duchenne carriers.
    Rugolo M, Rocchi M, Lenaz G, Romeo G.
    FEBS Lett; 1987 Feb 23; 212(2):313-6. PubMed ID: 3817163
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  • 20. [Use of dystrophin c-DNA for the direct diagnosis of Duchenne muscular dystrophy in female carriers].
    Baiget M, del Río E, Gallano P.
    Neurologia; 1989 Oct 23; 4(8):268-76. PubMed ID: 2576910
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