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European Journal of Human Genetics
Volumn 13, Issue 5, 2005, Pages 517-518
From chromosomes to DNA, a revolution in prenatal diagnosis
Author keywords

[No Author keywords available]
Indexed keywords

ANXIETY; AUTOMATION; BLOOD ANALYSIS; CHROMOSOME 13; CHROMOSOME 18; CHROMOSOME 21; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; COST EFFECTIVENESS ANALYSIS; CYTOGENETICS; DECISION MAKING; DEVELOPMENTAL DISORDER; DIAGNOSTIC ACCURACY; DIAGNOSTIC PROCEDURE; DIAGNOSTIC VALUE; DNA DETERMINATION; DNA MICROARRAY; DNA PROBE; DUCHENNE MUSCULAR DYSTROPHY; ECHOGRAPHY; EXON; FETUS ECHOGRAPHY; FLUORESCENCE IN SITU HYBRIDIZATION; GENE DELETION; GENE MUTATION; GENETIC SCREENING; HETEROZYGOTE DETECTION; HIGH RISK PREGNANCY; HUMAN; KARYOTYPE; MATERNAL AGE; NOTE; POLYMERASE CHAIN REACTION; PREDICTION; PREGNANCY; PRENATAL CARE; PRENATAL DIAGNOSIS; PRIORITY JOURNAL; QUANTITATIVE ANALYSIS; RISK BENEFIT ANALYSIS; SCREENING TEST; STANDARD; X CHROMOSOME; Y CHROMOSOME; ARTICLE; FEMALE; GENETIC COUNSELING; GENETICS; KARYOTYPING; METHODOLOGY;
EID: 18844375309     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201327     Document Type: Note
Times cited : (4)
References (7)
  • 2
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    • Rapid detection of common autosomal aneuploidies by quantitative fluorescent PCR on uncultured amniocytes
    • Rahil H, Solassol J, Philippe C, Lefort G, Jonveaux P: Rapid detection of common autosomal aneuploidies by quantitative fluorescent PCR on uncultured amniocytes. Eur J Hum Genet 2002; 10: 462-466.
    • (2002) Eur. J. Hum. Genet. , vol.10 , pp. 462-466
    • Rahil, H.1    Solassol, J.2    Philippe, C.3    Lefort, G.4    Jonveaux, P.5
  • 3
    • 1642544630 scopus 로고    scopus 로고
    • Rapid, high throughput prenatal detection of aneuploidy using a novel quantitative method (MLPA)
    • Slater HR, Bruno DL, Ren H, Pertile M, Schouten JP, Choo KH: Rapid, high throughput prenatal detection of aneuploidy using a novel quantitative method (MLPA). J Med Genet 2003; 40: 907-912.
    • (2003) J. Med. Genet. , vol.40 , pp. 907-912
    • Slater, H.R.1    Bruno, D.L.2    Ren, H.3    Pertile, M.4    Schouten, J.P.5    Choo, K.H.6
  • 4
    • 0141613852 scopus 로고    scopus 로고
    • Rapid and simple prenatal diagnosis of common chromosome disorders: Advantages and disadvantages of the molecular methods FISH and QF-PCR
    • Hulten MA, Dhanjal S, Pertl B: Rapid and simple prenatal diagnosis of common chromosome disorders: advantages and disadvantages of the molecular methods FISH and QF-PCR. Reproduction 2003; 126: 279-297.
    • (2003) Reproduction , vol.126 , pp. 279-297
    • Hulten, M.A.1    Dhanjal, S.2    Pertl, B.3
  • 5
    • 0038207040 scopus 로고    scopus 로고
    • Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalities
    • Grimshaw GM, Szczepura A, Hulten M et al: Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalities. Health Technol Assess 2003; 7: 1-146.
    • (2003) Health Technol. Assess. , vol.7 , pp. 1-146
    • Grimshaw, G.M.1    Szczepura, A.2    Hulten, M.3
  • 7
    • 0942278950 scopus 로고    scopus 로고
    • Cost utility of prenatal diagnosis and the risk-based threshold
    • Harris RA, Washington AE, Nease Jr RF, Kuppermann M: Cost utility of prenatal diagnosis and the risk-based threshold. Lancet 2004; 363: 276-282.
    • (2004) Lancet , vol.363 , pp. 276-282
    • Harris, R.A.1    Washington, A.E.2    Nease Jr., R.F.3    Kuppermann, M.4

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.