Detection of chromosome 11 alterations in blood and bone marrow by interphase cytogenetics in mantle cell lymphoma
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1995.tb08386.x/fullpdf
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1. Detection of chimeric BCR-ABL genes on bone marrow samples and blood smears in chronic myeloid and acute lymphoblastic leukemia by in situ hybridization
2. Circulating lymphoma cells in patients with B & T non-Hodgkin's lymphoma detected by immunoglobulin and T-cell receptor gene rearrangement
3. Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes
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1. The utility of interphase fluorescence in situ hybridization for the detection of the translocation t(11;14)(q13;q32) in the diagnosis of mantle cell lymphoma on fine-needle aspiration specimens;Cancer;2005-02-11
2. The role of molecular studies in lymphoma diagnosis: a review;Pathology;2004-02
3. Molecular basis of mantle cell lymphoma;British Journal of Haematology;2003-12-19
4. Mantle cell lymphoma: improved diagnostics using a combined approach of immunohistochemistry and identification of t(11;14)(q13;q32) by polymerase chain reaction and fluorescence in situ hybridization;Virchows Archiv;2003-05-01
5. Quantitation of Cyclin D1 Over-expression Using Competitive Fluorescent Reverse Transcription Polymerase Chain Reaction: A Tool for the Differential Diagnosis of Mantle Cell Lymphoma;Medical Oncology;2003
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