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Duchenne肌营养不良的产前诊断 被引量:2

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摘要 Duchenne肌营养不良(Duchenne muscular dystrophy,DMD,OMIM:#310200)又称假性肥大型肌营养不良,是常见的致死性X染色体连锁隐性遗传病之一,在活产男婴中的发生率为1/3500。
作者 马祎楠
出处 《中华围产医学杂志》 CAS 北大核心 2012年第10期595-598,共4页 Chinese Journal of Perinatal Medicine
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  • 2Mandel JI.. Dystrophin. The gene and its product. Nature, 1989, 339:584-586.
  • 3Yau SC, Bobrow M, Mathew CG, et al. Accurate diagnosis of carriers of deletions and duplications in Duchenne/Becker muscular dystrophy by fluorescent dosage analysis. J Med Genet, 1996, 33:550-558.
  • 4Desguerre I, Christov C, Mayer M, et al. Clinica heterogeneity of duchenne muscular dystrophy (DMD) definition of sub-phenotypes and predictive criteria by long term follow-up. PLoS One, 2009, 4:e4347.
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  • 9del Gaudio D, Yang Y, Boggs BA, et al. Molecular diagnosis of Duehenne/Becker muscular dystrophy: enhanced detection of dystrophin gene rearrangements by oligonucleotide array- comparative genomie hybridization. Hum Mutat, 2008, 29: 1100-1107.
  • 10Abbs S, Tuffery Giraud S, Bakker E, et al. Best practice guidelines on molecular diagnostics in Duchenne/Becker muscular dystrophies. Neuromuscul Disord, 2010, 20:422-427.

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