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Volumn 18, Issue 5, 2002, Pages 289-294

Fluorescence in situ hybridization (FISH) on uncultured amniocytes for diagnosis of frequent chromosomal disorders;Fluoreszenz-in-situ-Hybridisierung (FISH) an nichtkultivierten Amnionzellen zur diagnostik häufiger chromosomenstärungen

Author keywords

Amniotic fluid cells; Chromosomal aberration; Fluorescence in situ hybridization (FISH); Interphase cytogenetics

Indexed keywords

AMNION CELL; AMNION FLUID; ARTICLE; CELL CULTURE; CHROMOSOME ABERRATION; CHROMOSOME ANALYSIS; CHROMOSOME DISORDER; CYTOGENETICS; DNA PROBE; FLUORESCENCE IN SITU HYBRIDIZATION; GERMANY; HYBRIDIZATION; INTERPHASE; MEDICAL SOCIETY; PRENATAL DIAGNOSIS; SCREENING TEST;

EID: 0036923242     PISSN: 14346931     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00444-002-0348-0     Document Type: Article
Times cited : (1)

References (28)
  • 1
    • 0002848266 scopus 로고    scopus 로고
    • Interphase-FISH-test als schnelltest für trisomien im fruchtwasser - Ergebnisse einer prospektiven untersuchung
    • Bink K, Pauer HU, Bartels (2000) Interphase-FISH-Test als Schnelltest für Trisomien im Fruchtwasser - Ergebnisse einer prospektiven Untersuchung. Z Geburtsh Neonatol 204:8-13
    • (2000) Z Geburtsh Neonatol , vol.204 , pp. 8-13
    • Bink, K.1    Pauer, H.U.2    Bartels3
  • 2
    • 85046113353 scopus 로고    scopus 로고
    • Cross-hybridization of the chromosome 13/21 alpha satellite DNA probe to chromosome 22 in the prenatal screening of common aneuploidies by FISH
    • Blancato JK (1996) Cross-hybridization of the chromosome 13/21 alpha satellite DNA probe to chromosome 22 in the prenatal screening of common aneuploidies by FISH (letter to editor). Prenat Diagn 16:769-774
    • (1996) Prenat Diagn , vol.16 , pp. 769-774
    • Blancato, J.K.1
  • 3
    • 0028198442 scopus 로고
    • Evaluation of X, Y, 18 and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescence in situ hybridization
    • Cacheux V, Tachdjian G, Druart L et al. (1994) Evaluation of X, Y, 18 and 13/21 alpha satellite DNA probes for interphase cytogenetic analysis of uncultured amniocytes by fluorescence in situ hybridization. Prenat Diagn 14:79-86
    • (1994) Prenat Diagn , vol.14 , pp. 79-86
    • Cacheux, V.1    Tachdjian, G.2    Druart, L.3
  • 4
    • 0027474571 scopus 로고
    • The need to revaluate trisomy screening for advanced maternal age in pre-natal diagnosis
    • Clark BA, Kennedy K, Olson S (1993) The need to revaluate trisomy screening for advanced maternal age in pre-natal diagnosis. Am J Obstet Gynecol 168:812-816
    • (1993) Am J Obstet Gynecol , vol.168 , pp. 812-816
    • Clark, B.A.1    Kennedy, K.2    Olson, S.3
  • 5
    • 4243825819 scopus 로고    scopus 로고
    • Grundlage und bewertung des "pränatalen schnelltests (FISH)" an nichtkultivierten fruchtwasserzellen im 2. Trimenon
    • Deutsche Gesellschaft für Humangenetik (1998) Grundlage und Bewertung des "pränatalen Schnelltests (FISH)" an nichtkultivierten Fruchtwasserzellen im 2. Trimenon. MedGen 10:319
    • (1998) Medgen , vol.10 , pp. 319
    • Deutsche Gesellschaft für Humangenetik1
  • 6
    • 0012332467 scopus 로고    scopus 로고
    • Wie sicher ist der FISH-test? Der pränatale schnelltest und seine bedeutung für die klinische routine
    • Eiben B, Hammans W (1999) Wie sicher ist der FISH-Test? Der pränatale Schnelltest und seine Bedeutung für die klinische Routine. Gynäkologie und Geburtshilfe hautnah 1/1999:15-19
    • (1999) Gynäkologie und Geburtshilfe Hautnah , vol.1 , pp. 15-19
    • Eiben, B.1    Hammans, W.2
  • 7
    • 85067536062 scopus 로고    scopus 로고
    • False-negative finding in rapid interphase FISH analysis of uncultured amniotic cells
    • Eiben B, Trawicki W, Hammans W, Epplen JT (1999) False- negative finding in rapid interphase FISH analysis of uncultured amniotic cells. Prenat Diagn 19:891-892
    • (1999) Prenat Diagn , vol.19 , pp. 891-892
    • Eiben, B.1    Trawicki, W.2    Hammans, W.3    Epplen, J.T.4
  • 8
    • 0032774179 scopus 로고    scopus 로고
    • Rapid preanatal diagnosis of aneuploidies in uncultured amniocytes by fluorescence in situ hybridization
    • Eiben B, Trawicki W, Hammans W, Goebel R, Pruggmayer M, Epplen JT (1999) Rapid preanatal diagnosis of aneuploidies in uncultured amniocytes by fluorescence in situ hybridization. Fetal Diagn Ther 14:193-197
    • (1999) Fetal Diagn Ther , vol.14 , pp. 193-197
    • Eiben, B.1    Trawicki, W.2    Hammans, W.3    Goebel, R.4    Pruggmayer, M.5    Epplen, J.T.6
  • 9
    • 6844238527 scopus 로고    scopus 로고
    • Discordant karyotypes in CVS and amniocenteses using cytogenetic and Fluorescence in Situ Hybridisation (FISH) analyses
    • Eiben B, Trawicki W, Haupt A et al. (1998) Discordant karyotypes in CVS and amniocenteses using cytogenetic and Fluorescence in Situ Hybridisation (FISH) analyses. Prenat Diagn 18:B7-89
    • (1998) Prenat Diagn , vol.18
    • Eiben, B.1    Trawicki, W.2    Haupt, A.3
  • 10
    • 0012354838 scopus 로고    scopus 로고
    • Die fluoreszenz-in-situ-hybridisierung (FISH) an nichtkultivierten amnionzellen
    • Eiben B, Hammans W, Goebel R, Epplen JT (1998) Die Fluoreszenz-in-situ-Hybridisierung (FISH) an nichtkultivierten Amnionzellen. Dtsch Ärztebl 95:40-42
    • (1998) Dtsch Ärztebl , vol.95 , pp. 40-42
    • Eiben, B.1    Hammans, W.2    Goebel, R.3    Epplen, J.T.4
  • 11
    • 0030023839 scopus 로고    scopus 로고
    • Prenatal cytogenetic results from cases referred for 44 different types of abnormal ultrasound findings
    • Hanna JS, Neu RL, Lockwood DH (1996) Prenatal cytogenetic results from cases referred for 44 different types of abnormal ultrasound findings. Prenat Diagn 16:109-15
    • (1996) Prenat Diagn , vol.16 , pp. 109-115
    • Hanna, J.S.1    Neu, R.L.2    Lockwood, D.H.3
  • 12
    • 0026767687 scopus 로고
    • Importance of complete follow up of spontaneous fetal loss after amniocentesis and chorion villus sampling
    • Halliday JL, Lumley J, Sheffield U et al. (1992) Importance of complete follow up of spontaneous fetal loss after amniocentesis and chorion villus sampling. Lancet 1:886-890
    • (1992) Lancet , vol.1 , pp. 886-890
    • Halliday, J.L.1    Lumley, J.2    Sheffield, U.3
  • 13
    • 0027384766 scopus 로고
    • Cytogenetic diagnoses after chorionic villus sampling are less reliable in very high and very low risk pregnancies
    • Kennerknecht I, Barbi G, Wolf M et al. (1993) Cytogenetic diagnoses after chorionic villus sampling are less reliable in very high and very low risk pregnancies. Prenat Diagn 13:929-944
    • (1993) Prenat Diagn , vol.13 , pp. 929-944
    • Kennerknecht, I.1    Barbi, G.2    Wolf, M.3
  • 14
    • 0025779063 scopus 로고
    • Mosaicism and accuracy of prenatal cytogenetic diagnoses after chorionic villi sampling and placental biopsies
    • Miny P, Hammer P, Gerlach B et al. (1991) Mosaicism and accuracy of prenatal cytogenetic diagnoses after chorionic villi sampling and placental biopsies. Prenat Diagn 11:581-590
    • (1991) Prenat Diagn , vol.11 , pp. 581-590
    • Miny, P.1    Hammer, P.2    Gerlach, B.3
  • 15
    • 0026787127 scopus 로고
    • Ultrasonographically detectable markers of fetal chromosome abnormalities
    • Nicolaides KH, Snjiders RJ, Gosden CM et al. (1992) Ultrasonographically detectable markers of fetal chromosome abnormalities. Lancet 340:704-707
    • (1992) Lancet , vol.340 , pp. 704-707
    • Nicolaides, K.H.1    Snjiders, R.J.2    Gosden, C.M.3
  • 16
    • 0034111393 scopus 로고    scopus 로고
    • The clinical application ofinterphase FISH in prenatal diagnosis
    • Pergament E, Chen PX, Thangavelu M, Fiddler M (2000) The clinical application ofinterphase FISH in prenatal diagnosis. Prenat Diagn 20:215-220
    • (2000) Prenat Diagn , vol.20 , pp. 215-220
    • Pergament, E.1    Chen, P.X.2    Thangavelu, M.3    Fiddler, M.4
  • 17
    • 0031048551 scopus 로고    scopus 로고
    • Discordant direct and culture results following chorionic villus sampling and the diagnosis of a third cell line in the fetus
    • Phillips OP, Velagaleti GVN, Tharapel AT, Shulman LP (1997) Discordant direct and culture results following chorionic villus sampling and the diagnosis of a third cell line in the fetus. Prenat Diagn 17:170-172
    • (1997) Prenat Diagn , vol.17 , pp. 170-172
    • Phillips, O.P.1    Velagaleti, G.V.N.2    Tharapel, A.T.3    Shulman, L.P.4
  • 18
    • 0012309978 scopus 로고    scopus 로고
    • Genetische pränataldiagnostik
    • Propping P (1998) Genetische Pränataldiagnostik. Dtsch Ärztebl 95:38-39
    • (1998) Dtsch Ärztebl , vol.95 , pp. 38-39
    • Propping, P.1
  • 20
    • 0030966616 scopus 로고    scopus 로고
    • Cross-hybridization of the chromosome 13/21 alpha-satellite DNA to chromosome 22 or a rare polymorphism?
    • Tardy EP, Toth A (1997) Cross-hybridization of the chromosome 13/21 alpha-satellite DNA to chromosome 22 or a rare polymorphism? Prenat Diagn 18:487-490
    • (1997) Prenat Diagn , vol.18 , pp. 487-490
    • Tardy, E.P.1    Toth, A.2
  • 21
    • 0035016839 scopus 로고    scopus 로고
    • Prenatal diagnosis using interphase fluorescence in situ hybridization (FISH): 2-year multi-center retrospective study and review of the literature
    • Teppenberg J, Pettenati MJ, Rao PN et al. (2001) Prenatal diagnosis using interphase fluorescence in situ hybridization (FISH): 2-year multi-center retrospective study and review of the literature. Prenat Diagn 21:293-301
    • (2001) Prenat Diagn , vol.21 , pp. 293-301
    • Teppenberg, J.1    Pettenati, M.J.2    Rao, P.N.3
  • 22
    • 0034042125 scopus 로고    scopus 로고
    • An assessment of the use of interphase FISH with chromosome specific probes as an alternative to cytogenetics in prenatal diagnosis
    • Thein AT, Abdel-Fattah SA, Kyle PM, Soothill PW (2000) An assessment of the use of interphase FISH with chromosome specific probes as an alternative to cytogenetics in prenatal diagnosis. Prenat Diagn 20:275-280
    • (2000) Prenat Diagn , vol.20 , pp. 275-280
    • Thein, A.T.1    Abdel-Fattah, S.A.2    Kyle, P.M.3    Soothill, P.W.4
  • 23
    • 0035169209 scopus 로고    scopus 로고
    • Familial X centromere variant resulting in false-positive prenatal diagnosis of monosomy X by interphase FISH
    • Tsuchiya K, Schueler MG, Dev GV (2001) Familial X centromere variant resulting in false-positiv prenatal diagnosis of monosomy X by interphase FISH. Prenat Diagn 21:852-855
    • (2001) Prenat Diagn , vol.21 , pp. 852-855
    • Tsuchiya, K.1    Schueler, M.G.2    Dev, G.V.3
  • 24
    • 0034006176 scopus 로고    scopus 로고
    • Aneuploidiediagnostik mittels Fluoreszenz-insitu-Hybridisierung (FISH); stellenwert bei schwangerschaften mit erhöhtem risiko für chromosomenaberrationen
    • Ulmer R, Pfeiffer RA, Kollert A, Beinder E (2000) Aneuploidiediagnostik mittels Fluoreszenz-insitu-Hybridisierung (FISH); Stellenwert bei Schwangerschaften mit erhöhtem Risiko für Chromosomenaberrationen. Z Geburtsh Neonatol 204:1-7
    • (2000) Z Geburtsh Neonatol , vol.204 , pp. 1-7
    • Ulmer, R.1    Pfeiffer, R.A.2    Kollert, A.3    Beinder, E.4
  • 25
    • 0031979305 scopus 로고    scopus 로고
    • Detection of translocations involoving the Y-chromosome on prospective preantal screening of commom chromosomal aneuploidies by FISH
    • Verlinsky Y, Ginsberg N, Chmura M et al. (1998) Detection of translocations involoving the Y-chromosome on prospective preantal screening of commom chromosomal aneuploidies by FISH. Prenat Diagn 18:390-392
    • (1998) Prenat Diagn , vol.18 , pp. 390-392
    • Verlinsky, Y.1    Ginsberg, N.2    Chmura, M.3
  • 26
    • 0029121295 scopus 로고
    • Cross-hybridization of the chromosome 13/21 alpha-satellite DNA probe to chromosome 22 in prenatal screening for common chromosomal aneuploidies by FISH
    • Verlinsky Y, Ginsberg N, Chmura M et al. (1995) Cross-hybridization of the chromosome 13/21 alpha-satellite DNA probe to chromosome 22 in prenatal screening for common chromosomal aneuploidies by FISH. Prenat Diagn 15:831-834
    • (1995) Prenat Diagn , vol.15 , pp. 831-834
    • Verlinsky, Y.1    Ginsberg, N.2    Chmura, M.3
  • 27
    • 0035012869 scopus 로고    scopus 로고
    • Fluorescence in situ hybridization (FISH) for rapid detection of aneuploidy: Experience in 911 prenatal cases
    • Weremowicz S, Sandstorm DJ, Morton CC et al. (2001) Fluorescence in situ hybridization (FISH) for rapid detection of aneuploidy: experience in 911 prenatal cases. Prenat Diagn 21:262-269
    • (2001) Prenat Diagn , vol.21 , pp. 262-269
    • Weremowicz, S.1    Sandstorm, D.J.2    Morton, C.C.3
  • 28
    • 0032881737 scopus 로고    scopus 로고
    • Risk of false-positive prenatale diagnosis using interphase FISH testing: Hybridization of alpha satellite X probe to chromosome 19
    • Winsor EJT, Dyack S, Wood-Burgess EM, Ryan G (1999) Risk of false-positive prenatale diagnosis using interphase FISH testing: hybridization of alpha satellite X probe to chromosome 19. Prenat Diagn 19:832-836
    • (1999) Prenat Diagn , vol.19 , pp. 832-836
    • Winsor, E.J.T.1    Dyack, S.2    Wood-Burgess, E.M.3    Ryan, G.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.