𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Burkitt cell leukemia with abnormality of chromosome no. 1

✍ Scribed by Dr. H. D. Solomons; B. Mendelow; A. Levinstein; A. E. Johnson; R. Bernstein

Publisher
John Wiley and Sons
Year
1983
Tongue
English
Weight
284 KB
Volume
14
Category
Article
ISSN
0361-8609

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

Secondary nonrandom chromosomal abnormal
Secondary nonrandom chromosomal abnormalities of band 13q34 in burkitt lymphoma-leukemia
✍ Dr. Roland Berger; Maryvonne le Coniat; Josette DerrΓ©; Danielle Vecchione πŸ“‚ Article πŸ“… 1989 πŸ› John Wiley and Sons 🌐 English βš– 263 KB

Clonal abnormalities of the long arm of chromosome 13 were detected in 9 of 54 patients with Burkitt lymphoma-leukemia. All abnormalities involved band 13q34, in three patients as t(1;13). The 13q34 abnormalities are thus the second most frequent secondary chromosomal abnormalities, after those of c

Characteristic chromosomal abnormalities
Characteristic chromosomal abnormalities in biopsies and lymphoid-cell lines from patients with burkitt and non-burkitt lymphomas
✍ L. Zech; U. Haglund; K. Nilsson; G. Klein πŸ“‚ Article πŸ“… 1976 πŸ› John Wiley and Sons 🌐 French βš– 916 KB

## Abstract The karyotypes of cells from 10 Burkitt lymphoma (BL) biopsies, eight cell lines established from BL and nine cell lines from non‐BL sources were studied by chromosome banding techniques. With the exception of the BL‐derived cell lines BJAB, GC‐BJAB, Maku and U‐8691 all biopsies and lin

Genetic aberrations including chromosome
Genetic aberrations including chromosome 1 abnormalities and clinical features of plasma cell leukemia
✍ Hong Chang; Xiaoying Qi; Joanna Yeung; Donna Reece; Wei Xu; Bruce Patterson πŸ“‚ Article πŸ“… 2009 πŸ› Elsevier Science 🌐 English βš– 245 KB

Plasma cell leukemia (PCL) is a rare form of plasma cell malignancy, few large series reported underlying genetic abnormalities. We systematically evaluated the genomic aberrations in 41 PCL patients by combining fluorescence in situ hybridization with cytoplasmic light chain immunofluorescence and

Chromosome 21 abnormalities with AML1 am
Chromosome 21 abnormalities with AML1 amplification in acute lymphoblastic leukemia
✍ Maryvonne Busson-Le Coniat; Florence Nguyen Khac; Marie-ThΓ¨rΓ©se Daniel; Olivier πŸ“‚ Article πŸ“… 2001 πŸ› John Wiley and Sons 🌐 English βš– 142 KB

## Abstract Fluorescence in situ hybridization (FISH) studies were performed in three cases of acute lymphoblastic leukemia (ALL) with marker chromosomes to analyze the contribution of chromosome 21 in these markers. FISH with a chromosome 21 painting probe confirmed that chromosome 21 was involved