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Journal Abstract Search

225 related items for PubMed ID: 2563842

  • 1. Distinction of Becker from limb-girdle muscular dystrophy by means of dystrophin cDNA probes.
    Norman A, Thomas N, Coakley J, Harper P.
    Lancet; 1989 Mar 04; 1(8636):466-8. PubMed ID: 2563842
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  • 2. Intragenic deletions in 164 boys with Duchenne muscular dystrophy (DMD) studied with dystrophin cDNA.
    Upadhyaya M, Smith RA, Thomas NS, Norman AM, Harper PS.
    Clin Genet; 1990 Jun 04; 37(6):456-62. PubMed ID: 2200624
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  • 3. [Genetic studies of Duchenne muscular dystrophy families using the dystrophy families using the dystrophin cDNA].
    Saito K, Tanaka A, Harada T, Ikeya K, Fukuyama Y, Arahata K, Sugita H, Osawa M, Shishikura K, Suzuki H.
    No To Hattatsu; 1989 Jul 04; 21(4):361-8. PubMed ID: 2675944
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  • 4. Gene deletions in Japanese patients with Duchenne and Becker muscular dystrophies: deletion study and carrier detection.
    Asano J, Tomatsu S, Sukegawa K, Ikedo Y, Minami R, Iida M, Nishimura M, Nakagawa M, Ohshiro M, Orii T.
    Clin Genet; 1991 Jun 04; 39(6):419-24. PubMed ID: 1863988
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  • 5. Screening of deletions in the dystrophin gene with the cDNA probes Cf23a, Cf56a, and Cf115.
    Passos-Bueno MR, Rapaport D, Love D, Flint T, Bortolini ER, Zatz M, Davies KE.
    J Med Genet; 1990 Mar 04; 27(3):145-50. PubMed ID: 2182872
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  • 6. The diagnosis of Duchenne and Becker muscular dystrophies: two years' experience in a comprehensive carrier screening and prenatal diagnostic laboratory.
    Laing NG, Mears ME, Chandler DC, Layton MG, Thomas HE, Johnsen RD, Goldblatt J, Kakulas BA.
    Med J Aust; 1991 Jan 07; 154(1):14-8. PubMed ID: 1670611
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  • 7. Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations.
    Darras BT, Blattner P, Harper JF, Spiro AJ, Alter S, Francke U.
    Am J Hum Genet; 1988 Nov 07; 43(5):620-9. PubMed ID: 2903663
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  • 15. Is dystrophin always altered in Becker muscular dystrophy patients?
    Vainzof M, Passos-Bueno MR, Pavanello RC, Zatz M.
    J Neurol Sci; 1995 Jul 07; 131(1):99-104. PubMed ID: 7561956
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  • 16. 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 07; 36(3):211-27. PubMed ID: 1684391
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  • 17. Limb-girdle syndrome: a genetic study of 22 large Brazilian families. Comparison with X-linked Duchenne and Becker dystrophies.
    Passos-Bueno MR, Vainzof M, Pavanello Rde C, Pavanello-Filho I, Lima MA, Zatz M.
    J Neurol Sci; 1991 May 07; 103(1):65-75. PubMed ID: 1865235
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  • 18. Analysis of Scottish Duchenne and Becker muscular dystrophy families with dystrophin cDNA probes.
    Cooke A, Lanyon WG, Wilcox DE, Dornan ES, Kataki A, Gillard EF, McWhinnie AJ, Morris A, Ferguson-Smith MA, Connor JM.
    J Med Genet; 1990 May 07; 27(5):292-7. PubMed ID: 2191136
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  • 19. Improved diagnosis of Becker muscular dystrophy by dystrophin testing.
    Hoffman EP, Kunkel LM, Angelini C, Clarke A, Johnson M, Harris JB.
    Neurology; 1989 Aug 07; 39(8):1011-7. PubMed ID: 2668783
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  • 20. Frame-shift deletions in patients with Duchenne and Becker muscular dystrophy.
    Malhotra SB, Hart KA, Klamut HJ, Thomas NS, Bodrug SE, Burghes AH, Bobrow M, Harper PS, Thompson MW, Ray PN.
    Science; 1988 Nov 04; 242(4879):755-9. PubMed ID: 3055295
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