Cytogenetic and molecular diagnosis of chromosome 5 deletions in myelodysplasia
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2000.02285.x/fullpdf
Reference24 articles.
1. Use of a CEPH meiotic breakpoint panel to refine the locus of limb-girdle muscular dystrophy type 1A (LGMD1A) to a 2-Mb interval on 5q31;Bartoloni;Genomics,1998
2. Proposals for the classification of the myelodysplastic syndromes;Bennett;British Journal of Haematology,1982
3. Chromosomal deletions in myelodysplasia;Boultwood;Leukemia and Lymphoma,1995
4. Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q- syndrome: delineation of the critical region on 5q and identification of a 5q- breakpoint;Boultwood;Genomics,1994
5. Physical mapping of the minimal region of loss in 5q- chromosome;Fairman;Proceedings of the National Academy of Science of the United States of America,1995
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