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18-三体综合征1例

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作者 沈玉才
出处 《中国儿童保健杂志》 CAS 2006年第6期657-657,共1页 Chinese Journal of Child Health Care
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  • 1刘权章.人类染色体方法学[M].北京:人民卫生出版社,1992.269-271.
  • 2Tongsong T, Sirichotiyakul S, wanapirake et al. Sonographic features of trisomy 18 atmidpregnancy. J obstet Gynecol Res,2002, 28 (5), 245.
  • 3Carlson DE, Platt LD. The ultrasound teiad of fetal hydramnios abnormal hand posturing and any other anomaly predicts autosomal trisomy. Obstet Gynecol, 1992, 79 (4): 731.
  • 4Moran C J, Tay JB, Morrison JJ. Ultrasound detection and perinatal outcome of fetal trisomies 21, 18 and 13 in the absence of a routine fetal amonaly scan or biochemical screening . Ultrasound obstet Gynecol, 2002, 20 (5): 482.
  • 5Nyberg DA, Kramer D, Resta RG et al. Prenatal sonographic findings of trisomy 18: Reviewof 47 cases. J Ultrasound Med.1993, 12 (2): 103.
  • 6Shieds LE, Carpenter LA, Smith KM et al. Ultrasonographic diagnosis of trisomy 18: Is it practical in the early second trimester. J Ultrasound Med, 1998, 17 (5): 327.
  • 7Plomaki GE, Haddow JE, Knight GJ et al. Risk-based prenatal screening for trisomy 18 using alpha fetoprotein, unconjugated oestriol and human chorionic gonadotropin. Prenat diagn, 1995, 15(8): 713.
  • 8Yankowitz J, Fulton A, Williamson R et al. Prospective evaluation of prenatal maternal serum screening for trisomy 18. Am J Obstet Gynecol, 1998, 178 (3):446.

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