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Volumn 21, Issue 1, 2004, Pages 18-21

Prenatal Diagnosis of Chromosomal Abnormalities Through Amniocentesis

Author keywords

Amniocentesis; Chromosomal abnormalities; Prenatal diagnosis

Indexed keywords


EID: 85020949558     PISSN: 13417738     EISSN: 13475878     Source Type: Journal    
DOI: 10.1274/jmor.21.18     Document Type: Article
Times cited : (4)

References (12)
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  • 2
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  • 3
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    • National Institute of Child Health Development National Registry for Amniocentesis Study Group (1976): Midtrimester amniocentesis for prenatal diagnosis: safety and accuracy. JAMA 236, 1471-1476.
    • (1976) JAMA , vol.236 , pp. 1471-1476
  • 4
    • 0022650629 scopus 로고
    • Randmized controlled trial of genetic amniocentesis in 4,606 low-risk women
    • Tabor, A., Philip, J., Madsen, M.I., Bang, J., Obel, E.B. and Norgaard-Pedersen, B. (1986): Randmized controlled trial of genetic amniocentesis in 4,606 low-risk women. Lancet, 1, 1287-1293.
    • (1986) Lancet , vol.1 , pp. 1287-1293
    • Tabor, A.1    Philip, J.2    Madsen, M.I.3    Bang, J.4    Obel, E.B.5    Norgaard-Pedersen, B.6
  • 5
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    • Prenatal diagnostic techniques
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    • Goldberg, J.D. and Norton, M.E. (2001): Prenatal diagnostic techniques. In: The unborn patient, 3rd edition (Harrison, M.R. ed.), pp. 125-148, W.B. Saunders Company, Philadelphia.
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    • Goldberg, J.D.1    Norton, M.E.2
  • 6
    • 0002232454 scopus 로고
    • Prenatal diagnosis of chromosomal abnormalities through amniocentesis
    • 3rd edition (Milunsky, A., ed.) Johns Hopkins University Press, Baltimore
    • Hsu, L.Y.F. (1992): Prenatal diagnosis of chromosomal abnormalities through amniocentesis. In: Genetic disorders and the fetus, 3rd edition (Milunsky, A., ed.), pp. 179-248, Johns Hopkins University Press, Baltimore.
    • (1992) Genetic disorders and the fetus , pp. 179-248
    • Hsu, L.Y.F.1
  • 7
    • 0020370630 scopus 로고
    • Rates of trisomies 21, 18, 13 and other chromosome abnormalities in about 20,000 prenatal studies compared with estimated rates in live births
    • Schreinemachers, D.M., Cross, P.K. and Hook, E.B. (1981): Rates of trisomies 21, 18, 13 and other chromosome abnormalities in about 20,000 prenatal studies compared with estimated rates in live births. Hum. Genet., 61, 318-34.
    • (1981) Hum. Genet. , vol.61 , pp. 318-334
    • Schreinemachers, D.M.1    Cross, P.K.2    Hook, E.B.3
  • 8
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    • Japanese
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  • 9
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    • Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocation of chromosome 4
    • USA
    • Pinkel, D., Landegent, J., Collins, C., Fuscoe, J., Segraves, R., Lucas, J. and Gray, J. (1988): Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocation of chromosome 4. Proc. Natl. Acad. Sci. USA, 85, 9138-9142.
    • (1988) Proc. Natl. Acad. Sci. , vol.85 , pp. 9138-9142
    • Pinkel, D.1    Landegent, J.2    Collins, C.3    Fuscoe, J.4    Segraves, R.5    Lucas, J.6    Gray, J.7
  • 10
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    • Role of amniotic fluid interphase fluorescence in situ hybridization (FISH) analysis in patient management
    • Cheong Leung, W., Chitayat, D., Seaward, G., Windrim, R., Ryan, G., Barrett, J. and Winsor, E.J. (2001): Role of amniotic fluid interphase fluorescence in situ hybridization (FISH) analysis in patient management. Prenat. Diagn., 21, 327-332.
    • (2001) Prenat. Diagn. , vol.21 , pp. 327-332
    • Cheong, L.W.1    Chitayat, D.2    Seaward, G.3    Windrim, R.4    Ryan, G.5    Barrett, J.6    Winsor, E.J.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.