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Volumn 332, Issue 7539, 2006, Pages 452-454

Fetal nuchal translucency scan and early prenatal diagnosis of chromosomal abnormalities by rapid aneuploidy screening: Observational study

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; ANEUPLOIDY; ARTICLE; CHORION VILLUS SAMPLING; CHROMOSOME 13; CHROMOSOME 18; CHROMOSOME 21; CHROMOSOME ABERRATION; FETUS; HEALTH CARE COST; HEALTH CARE POLICY; HUMAN; KARYOTYPE; MAJOR CLINICAL STUDY; NUCHAL TRANSLUCENCY MEASUREMENT; POLYMERASE CHAIN REACTION; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; TRISOMY 21; X CHROMOSOME; Y CHROMOSOME;

EID: 33644777447     PISSN: 09598146     EISSN: None     Source Type: Journal    
DOI: 10.1136/bmj.38730.655197.AE     Document Type: Article
Times cited : (62)

References (12)
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    • Mann, K.1    Fox, S.P.2    Abbs, S.J.3    Yau, S.C.4    Scriven, P.N.5    Docherty, Z.6
  • 4
    • 0035081439 scopus 로고    scopus 로고
    • A large-scale evaluation of amnio-PCR for the rapid prenatal diagnosis of fetal trisomy
    • Levett LJ, Liddle S, Meredith R. A large-scale evaluation of amnio-PCR for the rapid prenatal diagnosis of fetal trisomy. Ultrasound Obstet Gynecol 2001;17:115-8.
    • (2001) Ultrasound Obstet Gynecol , vol.17 , pp. 115-118
    • Levett, L.J.1    Liddle, S.2    Meredith, R.3
  • 5
    • 0032951503 scopus 로고    scopus 로고
    • International, collaborative assessment of 146,000 prenatal karyotypes: Expected limitations if only chromosome-specific probes and fluorescent in-situ hybridization are used
    • Evans MI, Henry GP, Miller WA, Bui TH, Snidjers RJ, Wapner RJ, et al. International, collaborative assessment of 146,000 prenatal karyotypes: expected limitations if only chromosome-specific probes and fluorescent in-situ hybridization are used. Hum Reprod 1999;14:1213-6.
    • (1999) Hum Reprod , vol.14 , pp. 1213-1216
    • Evans, M.I.1    Henry, G.P.2    Miller, W.A.3    Bui, T.H.4    Snidjers, R.J.5    Wapner, R.J.6
  • 7
    • 0035968587 scopus 로고    scopus 로고
    • Prenatal detection of chromosome disorders by QF-PCR
    • Adinolfi M, Sherlock J. Prenatal detection of chromosome disorders by QF-PCR. Lancet 2001;358:1030-1.
    • (2001) Lancet , vol.358 , pp. 1030-1031
    • Adinolfi, M.1    Sherlock, J.2
  • 8
    • 0032146382 scopus 로고    scopus 로고
    • UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal translucency thickness at 10-14 weeks of gestation
    • Snijders RJM, Noble P, Sebire N, Souka A, Nicolaides KH. UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal translucency thickness at 10-14 weeks of gestation. Lancet 1998;351:343-6.
    • (1998) Lancet , vol.351 , pp. 343-346
    • Snijders, R.J.M.1    Noble, P.2    Sebire, N.3    Souka, A.4    Nicolaides, K.H.5
  • 11
    • 0036126106 scopus 로고    scopus 로고
    • The effect of fast reporting by amnio-PCR on anxiety levels in women with positive biochemical screening for Down syndrome - A randomized controlled trial
    • Leung WC, Lam YH, Wong Y, Lau ET, Tang MHY. The effect of fast reporting by amnio-PCR on anxiety levels in women with positive biochemical screening for Down syndrome-a randomized controlled trial. Prenat Diagn 2002;22:256-9.
    • (2002) Prenat Diagn , vol.22 , pp. 256-259
    • Leung, W.C.1    Lam, Y.H.2    Wong, Y.3    Lau, E.T.4    Mhy, T.5
  • 12
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    • Collaborative US data on prenatal diagnosis for parental carriers of chromosomal rearrangements: Risks of unbalanced progeny
    • Daniel A, ed. New York: Alan R Liss
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    • (1988) The Cytogenetics of Mammalian Autosomal Rearrangements , pp. 73-162
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.