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荧光原位杂交技术在无创性产前诊断中的应用 被引量:3

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摘要 产前诊断技术的发展趋势为早期、快速、准确、无创伤,能够在胚胎发育的较早期,安全、准确地对出生缺陷作出诊断。通过无创伤性的技术进行产前诊断是临床产前诊断的目标。荧光原位杂交(FISH)技术是一种具有高度灵敏性和特异性的染色体和基因分析技术,随着DNA技术的发展与染色体基因特异性探针的出现,目前广泛用于产前诊断各种染色体异常,尤其是在母血胎儿细胞遗传学诊断和胚胎植人前遗传学诊断中的应用,将无创性产前基因诊断水平提高到新的高度。
作者 许多 王晨虹
出处 《国际妇产科学杂志》 CAS 2008年第5期359-361,共3页 Journal of International Obstetrics and Gynecology
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  • 1[1]Shaffer LG,Bui TH.Molecular cytogenetic and rapid aneuploidy detection methods in prenatal diagnosis[J].Am J Med Genet C Semin Med Genet,2007,145(1):87-98.
  • 2[2]ten Kate LP.Rapid prenatal diagnosis of chromsomal abnormalities;limitations and possibilities[J].Ned Tijdschr Geneeskd,2006,150(29):1608-1612.
  • 3[3]Moatter T,Khilji Z,Murad F,et al.Analysis of anmiotic fluid specimens for common chromosome disorders using interphase fluorescence in situ hybridization[J].J Pak Med Assoc,2007,57(4):189-192.
  • 4[4]Babic I,Brajenovic-Milic B,Petrovie O,et al.Prenatal diagnosis of complete trisomy 19q[J].Prenat Diagn,2007,27 (7):644-647.
  • 5[5]Lissauer D,Larkins SA,Sharif S,et al.Prenatal diagnosis and prenatal imaging features of fetal monosomy 1p36[J].Prenat Diagn,2007,27 (9):874-878.
  • 6[6]Coccé MC,Villa O,Obregon MG,et al.Duplication dup (1)(q41q44) defined by fluorescence in situ hybridization:delineation of the 'trisomy 1q42→qter syndrome[J].Cytogenet Genome Res,2007,118(1):84-86.
  • 7[7]Vaglio A,Greif G,Bernal M,et al.Prenatal and postnatal characterization of a de novo Xq22.1 terminal deletion[J].Genet Test,2006,10(4):272-276.
  • 8[8]McClarren J,Donnenfeld AE,Ravnan JB.Prenatal diagnosis of an unexpected interstitial 22q11.2 deletion causing tnuncus arteriosus and thymic hypoplasia in a ring 22 chromosome derived from a maternally inherited paracentric inversion[J].Prenat Diagn,2006,26(13):1212-1215.
  • 9[9]Ozkinay F,Kanit H,Onay H,et al.Prenatal diagnosis of de novo unbalanced translocation 8p;21q using subtelomeric probes[J].Genet Couns,2006,17 (3):315-320.
  • 10[10]Bianchi DW,Simpson JL,Jackson LG,et al.Fetal gender and aneuploidy detection using fetal cells in maternal blood:analysis of NIFTY I data.National Institute of Child Health and Development Fetal Cell Isolation Study[J].Prenat Diagn,2002,22(7):609-615.

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