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荧光原位杂交在产前诊断中的应用及前景 被引量:5

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摘要 近年来,染色体荧光原位杂交(FISH)逐渐成为解决复杂的临床细胞遗传学问题的一项重要方法。在产科学研究中,它更是成为经典细胞遗传学的重要补充。本文就其在产前遗传咨询,孕期检测胎儿染色体异常及胚胎植入前产前诊断三方面的应用及前景进行探讨。
出处 《国外医学(妇产科学分册)》 2001年第5期259-261,共3页 Foreign Medical Sciences(Obstet Gynecol Fascicle)
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  • 1XuJ, Fong CT, Cedrone E, etal. Clin Genet, 1998, 53(6):490-496
  • 2BrackleyKJ, KilbyMD, Morton J, etal. Prenat Diagn, 1999, 19 (6): 570-574
  • 3Worthington S, Bower C, Harrop K, et al. J Paediatr Child Health, 1998, 34(5): 438-443
  • 4Feldman B, Edrahim SA, Hazan SL, et al. Am J Med Genet,2000, 90(3): 233-238
  • 5Toth A, Tardy EP, Hajdu K, et al. Eur J Obstet Gynecol Reprod Biol, 2001, 94(1): 46-50
  • 6Suzumori K, Tanemura M, Oya N, et al. Prenat Diagn, 1998, 18 (7): 725-730
  • 7Sawa R, Hayashi Z, Tanaka T, et al. J Obstet Gynaecol Res,2001, 27(1) :41-47
  • 8Cai LS, Lim AS, Tan A. Ann Acad Med Singapore, 1999, 28 ( 4 ): 502- 507
  • 9Bhatia SN, Suri V, Bundy A, et al. Prenat Diagn, 1999, 19(9):863-867
  • 10Serlachius M, Von Koskull H, Wessman M, et al. Prenat Diagn,2000, 20(5): 407-410

同被引文献24

  • 1潘涌.荧光原位杂交技术及其在白血病研究中应用的进展[J].国外医学(肿瘤学分册),1995,22(1):38-41. 被引量:1
  • 2Cremer T, Landegent J, Bruckner A, et al. Detection of chromosome aberrations in metaphase and interphase tumor cells in situ hybridization using chromosome specific library probes [ J ]. Hum Genet, 1986,74 : 346-352
  • 3Klinger K, Landes G, Shook D, et al. Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescencein situ hybridization (FISH) [ J ]. Am J Hum Genet, 1992,51:55-65
  • 4Ward BE, Gersen SL, Carelli MP, et al. Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization ;clinical experience with 4,500 specimens [J]. Am J Hum Genet, 1993,52:854-865
  • 5Witters I, Devriendt K, Legius E, et al. Rapid prenatal diagnosis of trisomy 21 in 5049 consecutive uncultured amniotic fluid samples by fluorescence in situ hybridisation (FISH) [ J]. Prenat Diagn,2002,22:29-33
  • 6Caine A, Mahby AE, Parkin CA, et al. Prenatal detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13,18,and 21 by FISH or PCR without a full karyotype; a cytogenetic risk assessment [ J ]. Lancet, 2005,366 : 123-128
  • 7Cremer T,Lanegent J,Brüuckner A,et al.Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques:Diagnosis of trisome 18 with probe L 1.84[J].Hum Genet,1986,74(4):346-352.
  • 8Lichter P,Cremer T,Tang CJ,et al.Rapid detection of human chromosome 21 aberraion by in situ hybridization[J].Proc Natl Acad Sci USA,1988,85(24):9664-9668.
  • 9Norio M,Robert G,Best S,et al.Nunerical chromosome abnormalities in spermatozoa of fertile and infertile men detected by fluorescence in situ hybridization[J].Hum Genet,1994,93(5):502-506.
  • 10Bryndorf T,Lundsteen C,Lamb A,et al.Rapid prenatal diagnosis of chromosme aneupadies by interphase fluorescence in situ hybrization:a one-year clinical experience with high-risk and urgent fetal and postnatal samples[J].Acta Obstet Gynecol Scand,2000,79(1):8-14.

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