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Catalog of chromosome aberrations in cancer
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TLDR
This poster presents a probabilistic procedure to count the number of chromosomes in the nucleus using a simple “spatially aggregating” procedure called “spot-spot analysis”.Abstract:
Chromosome 1-22 Chromosome X Chromosome Y Homogeneously Staining Regions (HSR) Ring Chromosomes (R) Double Minute Chromosomes (DMIN).read more
Citations
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Journal ArticleDOI
Chromosomes in the genesis and progression of ependymomas
TL;DR: Cytogenetic analysis was performed on cultures of primary ependymal tumors with different degrees of malignancy obtained from four patients, none of whom had received therapy before karyotypic evaluation, finding the most common abnormalities were monosomy 17 and 22 in four cases and losses of sex chromosomes in three cases.
Journal ArticleDOI
Cytogenetic studies in primary and metastatic neuroendocrine merkel cell carcinoma
Gabriella Sozzi,Maria Grazia Bertoglio,Silvana Pilotti,Franco Rilke,Marco A. Pierotti,Giuseppe Della Porta +5 more
TL;DR: Direct preparations of five primary and metastatic neuroendocrine Merkel cell carcinomas of the skin were analyzed using a G-banding technique and a recurrent structural abnormality was a rearranged chromosome #1 with involvement of p and q arms.
Journal ArticleDOI
Review of the cytogenetic changes in acute megakaryoblastic leukemia: one disease or several?
TL;DR: It is hypothesize that AMKL may represent at least three separate disease entities with different genetic alterations giving rise to similar, but not identical, disorders.
Book ChapterDOI
Neoplasia and cytogenetic abnormalities.
TL;DR: This chapter discusses the relationship between cytogenetic abnormalities and neoplasia, especially in the context of aneuploidy in the genesis and progression of neoplastic transformation.
Journal ArticleDOI
Detection of chromosome 20q deletions in bone marrow metaphases but not peripheral blood granulocytes in patients with myeloproliferative disorders or myelodysplastic syndromes
Fotios A. Asimakopoulos,Tracey L. Holloway,Elisabeth P. Nacheva,Michael A. Scott,Pierre Fenaux,Anthony R. Green +5 more
TL;DR: Seven patients with myeloproliferative disorders or myelodysplastic syndromes in whom a deletion of the long arm of chromosome 20 was detectable by G-banding and/or fluorescence in situ hybridization in most or all bone marrow metaphases are presented.