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非侵入性产前诊断方法的研究进展 被引量：1

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摘要 非侵入性产前诊断方法包括超声检查、母体血清标记物筛查、母体外周血中胎儿细胞的富集和分析、母体外周血中游离胎儿DNA的提取和分析等。各类技术近年来发展很快 。
作者 马建鸿 张元珍 胡伦颖 王燕
机构地区 武汉大学中南医院妇产科
出处 《国外医学（妇幼保健分册）》 2001年第4期157-159,共3页 Foreign Medical Sciences (Section of Maternal and Child Health)
关键词 产前诊断 胎儿有核红细胞 游离胎儿DNA
分类号 R714.5 [医药卫生—妇产科学]
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参考文献17

  • 1Lorenzo guariglia MD, Paolo Rosati MD. Isolated mild fetal pyelectasis detected by transvaginal sonography in advanced maternal age[J]. Obstect Gynecol, 1998, 92: 833-866.
  • 2Vintialeas AM, Campbell WA, Guzman ER, et al. Second trimester ultrasound markers for detection of trisomy 21: which markers are best[J]. Obstet Gynecol, 1997, 89: 942-944.
  • 3Katharine D, Wenstrom MD, John O, et al. α-Feta protein, free-β-Human chorionic gonadotropin and dimeric inhibin A produce the best resultsin a three-analyte, multiple-marker screening test for fetal Down syndrome[J]. Am J obstetGynecol, 1997, 177(5): 987-991.
  • 4Casals E, Aiber H, Martz JM, et al. First trimester biochemical markers for Down Syndrome[J]. Prenatal Diagen, 1999, 19:8-11.
  • 5Biagiotti B, Brizzi L, Periti E, et al. First trimester screening for Down's syndrome using maternal serum PAPP-A and free HCG in combination with fetal nuchal translucency thickness[J]. Br J obstet Gynecol, 1998, 105: 917-920.
  • 6Waohtel SS. Charge flow seperation:quantification of nucleated red blood cells in maternal blood during pregnancy[J]. Prenat Diagn, 1998, 18: 455-463.
  • 7Zhen DK, Wang JY, Falco VM, et al. Poly-FISH :a technique of repeated hybridizations that improves cytogenetic analysis of fetal cells in maternal blood[J]. Prenat Diagn, 1998, 18: 1181-1185.
  • 8Beatrice O, Genevieve L, Pierre B, et al. Fetal cells in maternal blood :the use of primed in situ (PRINS) labeling technique for fetal cell detection and sex assessment[J]. Prenat Diagn, 1998, 18: 1014-1022.
  • 9Chowdhary MR, Mathur R, Verma IC. Vtility of XY-amelogenin gene primers for detection of sex chromosome[J]. Indian J Med Res, 1998, 107(4): 182-186.
  • 10Lo YMD, Mark SCT, Tze KL, et al. Quantitive analysis of fetal DNA in maternal plasma and serum :implication for noninvasive prenatal diagnosis[J]. Am J Hum Genet, 1998, 62:768-775.

同被引文献17

  • 1李科生,蒲玮,朱军.计划生育技术服务人员有关神经管缺陷及其干预措施知晓率的调查[J].中国妇幼保健,2005,20(9):1133-1135. 被引量：3
  • 2Stoll C, Alembik Y, Dott B, et al. Impact of prenatal diagnosis on livebirth prevalence of children with congenital anomalies. Ann C, enet,2002, 45 (3) : 115 -121.
  • 3Peller AT, Westgate MN, Holmes LB. Trends in Congenital Malformations, 1974 - 1999 : Effect of Prenatal Diagnosis and Elective Termination. Obstetrics & Gynecology, 2004, 104(5) : 957 -964.
  • 4Hobbs CA, Hopkins SE, Simmons CJ. Sources of variability in birth defects prevalence rates. Teratology, 2001,64 ( Suppl 1 ) : 8 - 13.
  • 5International Clearinghouse for Birth Defects Monitoring Systems. Annual Report 2000. Rome: International Centre for Birth Defects, 2000.
  • 6De Vigan C, Bacna N, Cariati E, et al. Contribution of ultrasonographic examination to the prenatal detection of chromosomal abnormalities in 19 centres across Europe. Annales de C, enetique, 2001, 44(4) : 209 -217.
  • 7Siffel C, Correa A, Cragan J, et al. Prenatal diagnosis, pregnancy terminations and prevalence of Down syndrome in Atlanta. Birth Defects Research (Part A), 2004, 70:565 -571.
  • 8Cragan JD, Khoury MJ. Effect of prenatal diagnosis on epidemiologic studies of birth defects. Epidemiology, 2000, 11 (6) : 695 - 699.
  • 9Forrester MB, Merz RD, Yoon PW. Impact of prenatal diagnosis and elective termination on the prevalence of selected birth defects in Hawaii. Am J Epidemiol, 1998, 148(12): 1206-1211.
  • 10Centers for Disease Control and Prevention. Surveillance for Anencephaly and Spina Bifida and the Impact of Prenatal Diagnosis United States, 1985-1994. MMWR, 1995, 44(SS-4) : 1-13.

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国外医学（妇幼保健分册）
2001年 第4期

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