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Nature Genetics|April 1, 1996
Karyotyping human chromosomes by combinatorial multi-fluor FISHM R Speicher, S Gwyn Ballard, D C WardLaboratory Investigation; a Journal of Technical Methods and Pathology|May 20, 1999
Frequent chromosomal DNA unbalance in thyroid oncocytic (Hürthle cell) neoplasms detected by comparative genomic hybridizationG Tallini, A Hsueh, S Liu, et al.Cancer Research|March 1, 1995
Comparative genomic hybridization detects novel deletions and amplifications in head and neck squamous cell carcinomasM R Speicher, C Howe, P Crotty, et al.Cytogenetics and Cell Genetics|July 28, 2001
Classifying by colors: FISH-based genome analysisC Fauth, M R SpeicherLeukemia Research|April 1, 1993
Delineation of translocation t(15; 17) in acute promyelocytic leukemia by chromosomal in situ suppression hybridizationM R Speicher, A Jauch, A Parr, et al.American Journal of Medical Genetics|June 8, 2000
Breakpoint within the nucleolus organizer region resulting in a reciprocal translocation t (4;14)(q21;p12)M Grabowski, C Fauth, A Wirtz, et al.American Journal of Medical Genetics|September 25, 2001
Additional dark G-band in the p-arm of chromosome 19 due to a paracentric inversion with a breakpoint in the pericentromeric heterochromatinC Fauth, I Bartels, T Haaf, et al.Cytogenetics and Cell Genetics|July 7, 1999
A complete set of repeat-depleted, PCR-amplifiable, human chromosome-specific painting probesA Bolzer, J M Craig, T Cremer, et al.Pageof 27