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Histochemistry and Cell Biology|December 5, 1997
Single- and double-color oligonucleotide primed in situ labeling (PRINS): applications in pathologyL Wilkens, J Tchinda, P Komminoth, et al.
Virchows Archiv : an International Journal of Pathology|May 1, 1997
Detection of karyotype changes in interphase cells: oligonucleotide-primed in situ labelling versus fluorescence in situ hybridizationM Werner, L Wilkens, A Nasarek, et al.
Human Pathology|August 26, 1998
Analysis of hematologic diseases using conventional karyotyping, fluorescence in situ hybridization (FISH), and comparative genomic hybridization (CGH)L Wilkens, J Tchinda, D Burkhardt, et al.
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|December 5, 1997
Applications of single-color and double-color oligonucleotide primed in situ labeling in cytologyM Werner, A Nasarek, J Tchinda, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|February 12, 1998
Value of fluorescence in situ hybridization for detecting the bcr/abl gene fusion in interphase cells of routine bone marrow specimensM Werner, M Ewig, A Nasarek, et al.
Virchows Archiv : an International Journal of Pathology|June 2, 2000
Aberrations of chromosomes 5 and 8 as recurrent cytogenetic events in anaplastic carcinoma of the thyroid as detected by fluorescence in situ hybridisation and comparative genomic hybridisationL Wilkens, D Benten, J Tchinda, et al.
Der Urologe. Ausg. A|February 9, 2006
[Cytogenetic alterations in renal tumors. Applications for comparative genomic hybridization and fluorescence in situ hybridization]K D Mertz, J Tchinda, R Küfer, et al.
Cytogenetic and Genome Research|November 25, 2006
Array-based comparative genomic hybridization and copy number variation in cancer researchE K Cho, J Tchinda, J L Freeman, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|July 17, 1999
Cytogenetic aberrations in myelodysplastic syndrome detected by comparative genomic hybridization and fluorescence in situ hybridizationL Wilkens, D Burkhardt, J Tchinda, et al.
British Journal of Haematology|June 14, 2001
Spectral karyotyping and fluorescence in situ hybridization detect novel chromosomal aberrations, a recurring involvement of chromosome 21 and amplification of the MYC oncogene in acute myeloid leukaemia M2E Hilgenfeld, H Padilla-Nash, N McNeil, et al.
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