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胎儿染色体病的早期筛查 被引量:1

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出处 《中国优生与遗传杂志》 2004年第6期8-9,共2页 Chinese Journal of Birth Health & Heredity
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参考文献17

  • 1J.S.Oh,G.Wright,C.B.Coulam,et al.Gestational sac diameter in very early pregnancy as a predictor of fetal outcome[J]. Ultrasound Obstet Gynecol,2002,20:267-269.
  • 2Duguff L, Persutte W.H,Schultz L.K, Hobbins J.C,et al.Crown-rump length to yolk sac diameter ratio :A new method to predict fetal aneuploidy[J].Am J Obstet Gynecol,1998,178(1s):143s.
  • 3方群,安娜.B超筛查胎儿染色体非整倍体异常[J].中华妇产科杂志,2002,37(1):51-52. 被引量:22
  • 4M L Brizot,M H Carvalno,A.W Liao,et al. First-trimester screening for chromosomal abnormalities by fetal nuchal translucency in Brizilian population[J]. Ultrasound Obstet Gynecol,2001,18:652~655.
  • 5Cicerro S,Curcio P,Papageorghiou A,et al.Absence of nasal bone in fetuses with trisomy 21 at 11-14 weeks of gestation:an observation study[J]. Lancet,2001,358:1665-1667.
  • 6Otano L,Aiello H,Igarzabal L,et al.Association between first trimester absence of fetal nasal bone on ultrasound and Down's syndrome[J].Prenat Diagn,2002,22:930-932.
  • 7Orlandi F,Bilardo C.M,Campogrande M,et al.Measurement of nasal bone length at 11-14 weeks of pregnancy and its potential role in Down's syndrome risk asssesment[J].Ultrasound Obstet Gynecol, 2003,23(6):496~500.
  • 8Zoppi M.A,Ibba R.M,Axinan C,et al .Absence of fetal nasal bone and aneuploidies at first trimester nuchal translucency screening in 5425 unselected pregnancies[J].Prenat Diagn,2003,22(1):36~9.
  • 9Ginsberg N.A,Storm C,VerlinskyY.Cromn-rump lengths in missed miscarriages and trisomy 21[J].Blackwell Science,2001 ,18(5):488~490.
  • 10Haddow J.E,Palomaki G.E,Knight G.J,et al.Screening of maternal serum for fetal Down's syndrome in the first trimester[J]. N Engl J Med,1998,338:955-961.

二级参考文献19

  • 1Kubas C. Noninvasive means of identifying fetuses with possible Down syndrome: a review. J Perinat Neonatal Nurs, 1999,13:27-46.
  • 2Locatelli A, Piccoli MG, Vergani P, et al. Critical appraisal of the use of nuchal fold thickness measurements for the prediction of Down syndrome. Am J Obstet Gynecol, 2000,182:192-197.
  • 3Hafner E, Schuchter K, Liebhart E, et al. Results of routine fetal nuchal translucency measurement at weeks 10-13 in 4233 unselected pregnant women. Prenat Diagn, 1998,18:29-34.
  • 4Thilaganathan B, Olawaiye A, Sairam S, et al. Isolated fetal echogenic intracardiac foci or golf balls: is karyotyping for Down's syndrome indicated? Br J Obstet Gynecol, 1999,106:1294-1297.
  • 5Simpson J. The cardiac echogenic focus. Prenat Diagn,1999,19:972-975.
  • 6Farina A, Sekizawa A, Ralston SJ, et al. Latent class analysis applied to patterns of fetal sonographic abnormalities: definition of phenotypes associated with aneuploidy. Prenat Diagn, 1999, 19:840-845.
  • 7Roberts D, Walkinshaw SA, McCormack MJ, et al. Prenatal detection of trisomy 21: combined experience of two British hospitals. Prenat Diagn, 2000,20:17-22.
  • 8Grandjean H, Larroque D, Levi S, et al. Detection of chromosomal abnormalities, an outcome of ultrasound screening. The Eurofetus team. Ann NY Acad Sci, 1998,847:136-140.
  • 9Feuchtbaum LB, Currier RJ, Lorey FW, et al. Prenatal ultrasound findings in affected and unaffected pregnancies that are screen-positive for trisomy 18: the california experience. Prenat Diagn, 2000,20:293-299.
  • 10Shields LE, Carpenter LA, Smith KM, et al. Ultrasonographic diagnosis of trisomy 18: is it practical in the early second trimester? J Ultrasound Med,1998,17:327-331.

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