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加强对先天性心脏病诊治的研究

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作者 李万镇
出处 《中国医刊》 CAS 2003年第5期2-5,共4页 Chinese Journal of Medicine
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参考文献10

  • 1李树林,杨焕杰,李晔,白馨芝,田家玮,张贵寅.染色体22q11缺失与先天性心脏病[J].中华儿科杂志,2001,39(5):270-270. 被引量:1
  • 2惠慰.经食管超声心动图在先天性心脏病围术期中的运用[J].国外医学(心血管疾病分册),2002,29(3):156-158. 被引量:1
  • 3穆瑞斌.室间隔缺损的介入治疗进展[J].国外医学(心血管疾病分册),2002,29(6):349-351. 被引量:5
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  • 6Yamagishi H, Garg V, Matsuoka R, et al. A molecular pathway revealing a genetic basis for human cardiac and craniofacial defects.Science, 1999,283 : 1158 - 1161.
  • 7Momma K, Kondo C, Ando M, et al. Tetralogy of Fallot with chromosome 22q 11.2 deletion. Am J Cardiol, 1995,76 : 618 - 621.
  • 8Didier D, Ratib O, Beghetti M, et al. Morpholngic and functional evalution of congenital heart disease by magnetic resonance imaging. J Magn Reson Imaging, 1999,10:639 - 655.
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  • 10Hijazi ZM. Hakim F, Fadley F, et al. Transcatheler closure of single muscular ventricular septal defects using the amplatzer muscular VSD occluder. Catheter Cardiovasc Interv, 2000,49(2) : 167 - 170.

二级参考文献25

  • 1[1]Amplaz K, Moller JH. 《Radiology of congenital heart disease》. St. Louis: MO. Mosby, 1993:243~244
  • 2[2]Lloyd TR, Fedderly R, Mendelsohn AM. Circulation, 1993; 88(4 Pt 1): 1412~1420
  • 3[3]Latiff HA, Alwi M, Kandhavel G. Ann Thorac Surg, 1999; 68(4): 1400~1401
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  • 8[8]Hijazi ZM, Hakim F, Al-Fadley F. Catheter Cardiovase Interv, 2000; 49(2): 167~172
  • 9[9]Mullasari AS, Umesan CV, Krishnan U. Catheter Cardiovase Interv, 2001; 54(4): 484~487
  • 10[10]Gu X, Han YM, Titus JL. Catheter Cardiovase Interv, 2000; 50(4): 502~509

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