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血友病B患者及其携带者基因诊断新进展 被引量:2

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摘要 血友病B是X性连锁隐性遗传疾病 ,随着对其基因缺陷本质的认识及生物技术的发展 ,临床上已经能对患者及其携带者进行基因诊断及产前诊断 ,本文对此作一简要介绍。
出处 《国外医学(临床生物化学与检验学分册)》 2002年第3期133-134,158,共3页 Foreign Medical Sciences(section of Clinical Biochemistry and Laboratory Medicine
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参考文献13

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二级参考文献4

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共引文献18

同被引文献21

  • 1刘敬忠,陈怀华,张纪平,尹洪臣,曾淑燕,石奇珍,王海燕,Erica Vielhaber,Steve S.Sommer.27例乙型血友病患者Ⅸ因子基因突变研究[J].高技术通讯,1994,4(8):29-32. 被引量:3
  • 2王宁遂,邓兵,朱静.一种F Ⅸ基因多态性在我国人群中的检出[J].中华医学遗传学杂志,1994,11(4):217-218. 被引量:10
  • 3王宁遂,邓兵,朱静.应用多聚酶链反应和双链DNA循环测序对FIX基因点突变的研究[J].中华血液学杂志,1995,16(5):227-228. 被引量:7
  • 4刘敬忠,向华,刘亮,周航,张纪平,石奇珍,陈怀华,曾淑燕,S.S.Sommer.应用基因扩增转录测序技术诊断乙型血友病[J].中华医学杂志,1995,75(10):599-601. 被引量:8
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  • 9Garmen E,Pilar C,Satumino H,et al.Molecular analysisin hemophilia B families:identification of six new muta-tions in factorⅨgene[J].Haematologiea,2003,88(101):235-236.
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