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Journal Abstract Search

195 related items for PubMed ID: 2610487

  • 1. Molecular deletion patterns in Duchenne muscular dystrophy patients.
    Lucotte G, David F, Levy C.
    Ann Genet; 1989; 32(4):214-9. PubMed ID: 2610487
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  • 4. Preferential deletion of exons in Duchenne and Becker muscular dystrophies.
    Forrest SM, Cross GS, Speer A, Gardner-Medwin D, Burn J, Davies KE.
    Nature; 1989; 329(6140):638-40. PubMed ID: 2821406
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  • 5. 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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  • 6. DNA analysis of Duchenne and Becker muscular dystrophy using pERT87 genomic probes and dystrophin cDNA probes--establishing the optimum strategy for carrier diagnosis in the Japanese population.
    Ubagai T, Katayama S.
    Jinrui Idengaku Zasshi; 1991 Sep; 36(3):211-27. PubMed ID: 1684391
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  • 7. Possibilities and limitations of carrier diagnosis in families with Duchenne muscular dystrophy caused by deletions in the major hot spot region using pulsed-field gel electrophoresis.
    Huschenbett J, Volz A, Pfeifer L, Speer A.
    Biomed Biochim Acta; 1991 Sep; 50(12):1205-12. PubMed ID: 1824538
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  • 8. Southern blot and PCR analyses of dystrophin gene deletions in Japanese patients with Duchenne muscular dystrophy.
    Nakajima T, Matsuo M, Nakamura H, Fujiwara Y.
    Kobe J Med Sci; 1991 Feb; 37(1):21-33. PubMed ID: 1921260
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  • 9. Relatively low proportion of dystrophin gene deletions in Israeli Duchenne and Becker muscular dystrophy patients.
    Shomrat R, Gluck E, Legum C, Shiloh Y.
    Am J Med Genet; 1994 Feb 15; 49(4):369-73. PubMed ID: 8160727
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  • 11. Deletion analysis of Duchenne muscular dystrophy using cDNA probes and multiplex PCR.
    Radosavljević D, Todorović D, Crkvenjakov R.
    Neurol Croat; 1991 Feb 15; 40(3):157-64. PubMed ID: 1681950
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  • 13. Pathogenic and nonpathogenic deletions in two families with Duchenne muscular dystrophy.
    Hart KA, Abbs S, Bobrow M.
    Am J Med Genet; 1989 May 15; 33(1):142-5. PubMed ID: 2750784
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  • 14. Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophy.
    Kunkel LM, Hejtmancik JF, Caskey CT, Speer A, Monaco AP, Middlesworth W, Colletti CA, Bertelson C, Müller U, Bresnan M, Shapiro F, Tantravahi U, Speer J, Latt SA, Bartlett R, Pericak-Vance MA, Roses AD, Thompson MW, Ray PN, Worton RG, Fischbeck KH, Gallano P, Coulon M, Duros C, Boue J, Junien C, Chelly J, Hamard G, Jeanpierre M, Lambert M, Kaplan JC, Emery A, Dorkins H, McGlade S, Davies KE, Boehm C, Arveiler B, Lemaire C, Morgan GJ, Denton MJ, Amos J, Bobrow M, Benham F, Boswinkel E, Cole C, Dubowitz V, Hart K, Hodgson S, Johnson L, Walker A, Roncuzzi L, Ferlini A, Nobile C, Romeo G, Wilcox DE, Affara NA, Ferguson-Smith MA, Lindolf M, Kaariainen H, de la Chapelle A, Ionasescu V, Searby C, Ionasescu R, Bakker E, van Ommen GJ, Pearson PL, Greenberg CR, Hamerton JL, Wrogemann K, Doherty RA, Polakowska R, Hyser C, Quirk S, Thomas N, Harper JF, Darras BT, Francke U.
    Nature; 1989 May 15; 322(6074):73-7. PubMed ID: 3014348
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  • 15. Molecular deletion patterns in Duchenne and Becker type muscular dystrophy.
    Liechti-Gallati S, Koenig M, Kunkel LM, Frey D, Boltshauser E, Schneider V, Braga S, Moser H.
    Hum Genet; 1989 Mar 15; 81(4):343-8. PubMed ID: 2784778
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  • 16. Isolation of candidate cDNAs for portions of the Duchenne muscular dystrophy gene.
    Monaco AP, Neve RL, Colletti-Feener C, Bertelson CJ, Kurnit DM, Kunkel LM.
    Nature; 1989 Mar 15; 323(6089):646-50. PubMed ID: 3773991
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  • 20. Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophy.
    Rapaport D, Passos-Bueno MR, Brandão L, Love D, Vainzof M, Zatz M.
    Am J Med Genet; 1991 Jun 15; 39(4):437-41. PubMed ID: 1877622
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