A new rapid test (fluorescence in situ hybridisation [FISH]) in the prenatal diagnosis of the most common chromosomal aberrations: What is their practical value?;Ein neuer schnelltest (FISH) zur pranatalen diagnostik der haufigsten chromosomen-aberrationen - Welche Bedeutung hat er fur die praxis?

Deutsche Medizinische Wochenschrift

Volumn 123, Issue 3, 1998, Pages 55-57

  Eiben, B ^a   Hammans, W ^a   Goebel, R ^a   Epplen, J T ^b  

^a Evangelischen Krakenhaus   (Germany)

^b RUHR UNIVERSITY BOCHUM   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

CHROMOSOME ABERRATION; DIAGNOSTIC VALUE; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; PRENATAL DIAGNOSIS; SHORT SURVEY;

EID: 0032536051     PISSN: 00120472     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2007-1023898     Document Type: Short Survey

References (8)

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2. Eiben, B., U. Sancken: Computer software programs and Down's syndrome risk calculations. Lancet 347 (1996), 1553-1554.
3. Eiben, B., W. Trawicki, A. Haupt, S. Kasper, D. Wenger, B. Baier, W. Hammans: Discordant karyotypes in CVS and amniocenteses using cytogenetic and Fluorescence in Situ Hybridisation (FiSH) analyses. Prenat. Diagn. (1997) (in press).
4. Eiben, B., W. Hammans, S. Hansen, W. Trawicki, B. Osthelder, A. Stelzer, K.-D. Jaspers, R. Goebel: On the complication risk of early amniocentesis versus standard amniocentesis. Fet. Diagn. Ther. 12 (1997), 140-144.
5. Fritz, B., B. van Oorschot, E. Latta, H. Rehder: Möglichkeit falsch-negativer Befunde beim Trisomie 21 Screening. Z. Geburtsh. Neonatol. 200 (1996), 191-198.
6. Klinger, K., G. Landes, D. Shook, R. Harvey, C. Lopez, L. Locke, R. Osathanondh, B. Leverone, T. Houseal, K. Pavelka, W. Dackowski: Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH). Amer. J. Hum. Genet. 51 (1992), 55-65.
7. Verlinsky, N., N. Ginsberg, M. Chmura, M. Freidine, M. White, M. Strom, A. Kuliev: Crosshybridization of the chromosome 13/21 alpha satellite DNA probe to chromosome 22 in the screening of common chromosomal aneuploidies by FISH. Prenat. Diagn. 15 (1995), 831-834.
8. Ward, B. E., S. I. Gersen, M. Carelli, N. M. McGuire, W. R. Dackowski, M. Weinstein, C. Sandlin, R. Waren, K. Klinger: Rapid prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization. Clinical experience with 4500 specimens. Amer. J. Hum. Genet. 56 (1993), 854-865.