Cytogenetic study of Brazilian patients with Myelodysplastic Syndrome (MDS)

6Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

Abstract

Bone marrow cytogenetic studies were performed on 93 patients with primary myelodysplastic syndrome (MDS) diagnosed at the Clinical Hospital of the Federal University of Paraná, Brazil. Chromosomal alterations were observed in 69% of the patients. Monosomy of chromosome 7, deletions of 7q, 5q, 12p and 20q, rearrangements of 11q23 and trisomies of chromosomes 8 and 21 were the most frequent abnormalities observed. Among adult patients the most frequent aberrations were rearrangements of 11 q23 and 12p deletions. In the pediatric group, 5q deletions and monosomy of chromosome 7 were the most common alterations. Copyright by the Brazilian Society of Genetics.

Cite

CITATION STYLE

APA

Borgonovo, T., Ribeiro, E. M. S. F., Cornélio, D. A., Schmid-Braz, A. T., Jamur, V. R., Wuicik, L., … Cavalli, I. J. (2005). Cytogenetic study of Brazilian patients with Myelodysplastic Syndrome (MDS). Genetics and Molecular Biology, 28(4), 654–660. https://doi.org/10.1590/S1415-47572005000500002

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free