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Journal Abstract Search

240 related items for PubMed ID: 2180286

  • 21. 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; 39(6):419-24. PubMed ID: 1863988
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  • 22. Duchenne muscular dystrophy in a girl identified by dystrophin deficiency.
    Maytal J, Shanske AL, Fox JE, Lipper S, Eviatar L.
    Neuropediatrics; 1991 Aug; 22(3):163-5. PubMed ID: 1944823
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  • 24. Variability in clinical, genetic and protein abnormalities in manifesting carriers of Duchenne and Becker muscular dystrophy.
    Bushby KM, Goodship JA, Nicholson LV, Johnson MA, Haggerty ID, Gardner-Medwin D.
    Neuromuscul Disord; 1993 Jan; 3(1):57-64. PubMed ID: 8329890
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  • 28. Genetic counseling of isolated carriers of Duchenne muscular dystrophy.
    Hoffman EP, Pegoraro E, Scacheri P, Burns RG, Taber JW, Weiss L, Spiro A, Blattner P.
    Am J Med Genet; 1996 Jun 28; 63(4):573-80. PubMed ID: 8826437
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  • 30. X-chromosome methylation in manifesting and healthy carriers of dystrophinopathies: concordance of activation ratios among first degree female relatives and skewed inactivation as cause of the affected phenotypes.
    Azofeifa J, Voit T, Hübner C, Cremer M.
    Hum Genet; 1995 Aug 28; 96(2):167-76. PubMed ID: 7635465
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  • 32. Female monozygotic twins discordant for hemophilia A due to nonrandom X-chromosome inactivation.
    Bennett CM, Boye E, Neufeld EJ.
    Am J Hematol; 2008 Oct 28; 83(10):778-80. PubMed ID: 18645989
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  • 37. X-chromosome inactivation in monozygotic twins with systemic lupus erythematosus.
    Huang Q, Parfitt A, Grennan DM, Manolios N.
    Autoimmunity; 1997 Oct 28; 26(2):85-93. PubMed ID: 9546817
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  • 38. Muscle X-inactivation patterns and dystrophin expression in Duchenne muscular dystrophy carriers.
    Matthews PM, Benjamin D, Van Bakel I, Squier MV, Nicholson LV, Sewry C, Barnes PR, Hopkin J, Brown R, Hilton-Jones D.
    Neuromuscul Disord; 1995 May 28; 5(3):209-20. PubMed ID: 7633186
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  • 39. 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 28; 37(1):21-33. PubMed ID: 1921260
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  • 40. 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 28; 44(2):270-81. PubMed ID: 2643315
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