Workpackage

Research Activities of Project 11: Cytogenetics

Created by: Hellenbrecht (ELIC) , generated 2006/03/14, last changed: 2008/01/14

Call for collaborations

Collection of new recurring or rare chromosome aberrations

One of the major aims of this project is the collection of new recurring and/or rare chromosome aberrations. Cases of interest shall be :
- recurrent (i.e. previously described in at least 1 case),
- rare (previously described in less than 30 cases),
with well documented clinics and laboratory findings including images of the chromosome findings in cases of hematological malignancy, which were previously unpublished. These cases will be published in the Atlas of Genetics and Cytogenetics in Oncology and Haematology in collaboration between the Atlas and the European LeukemiaNet - Workpackage 11. Guidelines for authors may be found at the Atlas.

A list of rare recurring chromosome aberrations is available at the Atlas of Genetics and Cytogenetics in Oncology and Haematology .

Note : The Atlas is indexed in the Current Contents, and case reports in the Atlas are recorded in Mitelman's database of Chromosome Aberrations in Cancer

Lists of rare chromosome aberrations

Rare_chromosome_aberrations.pdf
Rare_chromosome_aberrations_II.pdf
Rare_chromosome_aberrations_III.pdf
Rare_chromosome_aberrations_IV.pdf

Molecular studies of chromosome aberrations

11p15/NUP98 project (Christina Mecucci)

 

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