A rare case of myelodysplastic syndrome with i(9q) in a child associated to osteochondromatosis-Reference-Cited by-同舟云学术

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A rare case of myelodysplastic syndrome with i(9q) in a child associated to osteochondromatosis

Published:2011-10-18 Issue:2 Volume:58 Page:308-309
ISSN:1545-5009
Container-title:Pediatric Blood & Cancer
language:en
Short-container-title:Pediatr. Blood Cancer

Author:

de Souza Daiane Corrêa,Fernandez Teresa de Souza,Land Marcelo G.,Marques Mario,Maioli Maria C.,Ornellas Maria H.,Costa Elaine S.

Funder

CNPq/Brazilian Ministry of Science and Technology

Brazilian Ministry of Health

Rio de Janeiro Research Support Foundation (FAPERJ), Brazil

Publisher

Wiley

Subject

Oncology,Hematology,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pbc.23272/fullpdf

Reference7 articles.

1. A pediatric approach to the WHO classification of myelodysplastic and myeloproliferative diseases;Hasle;Leukemia,2003

2. Cytogenetic biclonality in a child with hypocellular primary myelodysplastic syndrome;Rodrigues;Cancer Genet Cytogenet,2007

3. Multiple osteochondromas: Mutation update and description of the multiple osteochondromas mutation database (MOdb);Jennes;Hum Mutat,2009

4. Inhibition of osteoclast function reduces hematopoietic stem cell numbers in vivo;Lymperi;Blood,2011

5. Isochromosome in neoplasia;Mertens;Genes Chromosomes Cancer,1994

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