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Eine Ebene höherGruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 8
1993
Ried, Thomas; Lengauer, Christoph; Lipp, Martin; Fischer, C.; Cremer, Thomas und Ward, D. C.
(1993):
Evaluation of the utility of interphase cytogenetics to detect residual cells with a malignant genotype in mixed cell populations: a Burkitt lymphoma model.
In: DNA and cell biology, Bd. 12, Nr. 7: S. 637-643
[PDF, 1MB]
1991
Lichter, Peter; Boyle, A. L.; Cremer, Thomas und Ward, D. C.
(1991):
Analysis of genes and chromosomes by non-isotopic in situ hybridization.
In: Genetic analysis, Bd. 8: S. 24-35
[PDF, 2MB]
1990
Lichter, Peter; Jauch, Anna; Cremer, Thomas und Ward, D. C.
(1990):
Detection of Down syndrome by in situ hybridization with chromosome 21 specific DNA probes.
Sixth Annual National Down Syndrome Society Symposium, New York, USA, 7. - 8. Dezember 1989.
Patterson, David (Hrsg.):
In: Molecular genetics of chromosome 21 and down syndrome, Progress in clinical and biological research
Bd. 360
S. 69-78
[PDF, 1MB]
Ward, D. C.; Lichter, Peter; Cremer, Thomas; Borden, J. und Manuelidis, L.
(1990):
Human chromosome specific probes for the analysis of genetic and neoplastic disease.
3. International Congress on Automation and New Technology in Clinical Laboratory, Kobe, Japan, 5. - 8. September 1988.
Okuda, Kiyoshi (Hrsg.):
In: Automation and new technology in the clinical laboratory,
Oxford: Wiley-Blackwell. S. 145-150
[PDF, 1MB]
1988
Lichter, Peter; Cremer, Thomas; Borden, J.; Manuelidis, L. und Ward, D. C.
(1988):
Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries.
In: Human Genetics, Bd. 80, Nr. 3: S. 224-234
[PDF, 1MB]
Cremer, Thomas; Lichter, Peter; Borden, J.; Ward, D. C. und Manuelidis, L.
(1988):
Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes.
In: Human Genetics, Bd. 80, Nr. 3: S. 235-246
[PDF, 1MB]
Lichter, Peter; Cremer, Thomas; Tang, C. C.; Watkins, P. C.; Manuelidis, L. und Ward, D. C.
(1988):
Rapid detection of human chromosome 21 aberrations by in situ hybridization.
In: Proceedings of the National Academy of Sciences of the United States of America, Bd. 85, Nr. 24: S. 9664-9668
[PDF, 5MB]
1987
Singer, R. H.; Lawrence, J. B.; Langevin, G. L.; Rashtchian, R. N.; Villnave, C. A.; Cremer, Thomas; Tesin, D.; Manuelidis, L. und Ward, D. C.
(1987):
Double labelling in situ hybridization using non-isotopic and isotopic detection.
In: Acta histochemica et cytochemica, Bd. 20: S. 589-599
[PDF, 1MB]