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Number of items: 13.

Article

Manoir, Stanislas du and Speicher, Michael R. and Joos, Stefan and Schröck, Evelin and Popp, Susanne and Döhner, Hartmut and Kovacs, Gyula and Robert-Nicoud, Michel and Lichter, Peter and Cremer, Thomas (1993): Detection of complete and partial chromosome gains and losses by comparative genomic in situ hybridization. In: Human Genetics, Vol. 90, No. 6: pp. 590-610

Popp, Susanne and Jauch, Anna and Schindler, Detlev and Speicher, Michael R. and Lengauer, Christoph and Donis-Keller, Helen and Riethman, Harold C. and Cremer, Thomas (1993): A strategy for the characterization of minute chromosome rearrangements using multiple color fluorescence in situ hybridization with chromosome-specific DNA libraries and YAC clones. In: Human Genetics, Vol. 92, No. 6: pp. 527-532

Lengauer, Christoph and Speicher, Michael R. and Popp, Susanne and Jauch, Anna and Taniwaki, Masafumi and Nagaraja, Ramaiah and Riethman, Harold C. and Donis-Keller, Helen and D'Urso, Michele and Schlessinger, David and Cremer, Thomas (1993): Chromosomal bar codes produced by multicolor fluorescence in situ hybridization with multiple YAC clones and whole chromosome painting probes. In: Human Molecular Genetics, Vol. 2: pp. 505-512

Taniwaki, Masafumi and Speicher, Michael R. and Lengauer, Christoph and Jauch, Anna and Popp, Susanne and Cremer, Thomas (1993): Characterization of two marker chromosomes in a patient with acute nonlymphocytic leukemia by two-color fluorescence in situ hybridization. In: Cancer Genetics and Cytogenetics, Vol. 70, No. 2: pp. 99-102

Wessman, M. and Popp, Susanne and Ruutu, Tapani and Volin, L. and Cremer, Thomas and Knuutila, Sakari (1993): Detection of residual host cells after bone marrow transplantation using non-isotopic in situ hybridization. In: Bone Marrow Transplantation, Vol. 11: pp. 279-284

Tiainen, Marianne and Knuutila, Sakari and Popp, Susanne and Emmerich, Patricia and Cremer, Thomas and Parlier, Valerie and Jotterand Bellomo, Martine and Ruutu, Tapani (1992): Chromosomal in situ suppression hybridization of immunologically classified mitotic cells in hematologic malignancies. In: Genes, Chromosomes and Cancer, Vol. 4, No. 2: pp. 135-140

Popp, Susanne and Cremer, Thomas (1992): Development of a Biological Dosimeter for Translocation Scoring Based on Two-Color Fluorescence in Situ Hybridization of Chromosome Subsets. In: Journal of Radiation Research, Vol. 33: pp. 61-70

Popp, Susanne and Jauch, Anna and Qiu, Jing Ying and Smialek, Barbara and Cremer, Thomas and Becher, Reinhard (1991): Translocation (8;21) in acute nonlymphocytic leukemia delineated by chromosomal in situ suppression hybridization. In: Cancer Genetics and Cytogenetics, Vol. 57, No. 1: pp. 103-107

Popp, Susanne and Scholl, Hans Peter and Loos, Peter and Jauch, Anna and Stelzer, Ernst and Cremer, Christoph and Cremer, Thomas (1990): Distribution of chromosome 18 and X centric heterochromatin in the interphase nucleus of cultured human cells. In: Experimental Cell Research, Vol. 189, No. 1: pp. 1-12

Cremer, Thomas and Popp, Susanne and Emmerich, Patricia and Lichter, Peter and Cremer, Christoph (1990): Rapid metaphase and interphase detection of radiation-induced chromosome aberrations in human lymphocytes by chromosomal suppression in situ hybridization. In: Cytometry, Vol. 11, No. 1: pp. 110-118

Popp, Susanne and Remm, B. and Hausmann, Michael and Lührs, H. and van Kaick, G. and Cremer, Thomas and Cremer, Christoph (1990): Towards a cumultative biological dosimeter based on chromosome painting and digital image analysis. In: Kerntechnik, Vol. 55, No. 4: pp. 204-210

Book Section

Cremer, Christoph and Hausmann, Michael and Popp, Susanne and Cremer, Thomas (1993): Analyse von Strahlenschäden in menschlichen Metaphasechromosomen nach fluoreszenz in situ Hybridisierung. In: Arndt, Dietrich (ed.) : Zytogenetische Methoden. BGA-Schriften, Vol. 3. München: MMV. pp. 27-32

Cremer, Thomas and Lichter, Peter and Popp, Susanne and Schröck, Evelin and Jauch, Anna and Manoir, Stanislas du and Joos, Stefan and Lengauer, Christoph and Scherthan, Harry and Ried, Thomas and Speicher, Michael R. (1993): Detection of genetic imbalances in tumor genomes by fluorescence in situ hybridization with tumor genomic DNA and subregional DNA probes. In: Obe, Günter and Natarajan, Adayapalam T. (eds.) : Chromosomal alterations. Berlin u.a.: Springer. pp. 42-49

This list was generated on Wed Jul 23 23:45:04 2014 CEST.