Molecular markers for the diagnosis of Philadelphia chromosome negative myeloproliferative disorders
- 30 June 2004
- journal article
- review article
- Published by Elsevier in Pathologie Biologie
- Vol. 52 (5) , 267-274
- https://doi.org/10.1016/j.patbio.2003.09.019
Abstract
No abstract availableKeywords
This publication has 54 references indexed in Scilit:
- Endogenous BFU-E in peripheral blood in diagnosis of polycythemia veraEuropean Journal of Haematology, 2009
- Erythroid expansion mediated by the Gfi-1B zinc finger protein: role in normal hematopoiesisBlood, 2002
- Rapid determination of clonality by detection of two closely-linked X chromosome exonic polymorphisms using allele-specific PCR.Journal of Clinical Investigation, 1997
- Frequency of clonal remission in acute myeloid leukaemiaThe Lancet, 1993
- Molecular basis of mucopolysaccharidosis type II: Mutations in the iduronate-2-sulphatase geneHuman Mutation, 1993
- Chromosome Studies in 104 Patients With Polycythemia VeraMayo Clinic Proceedings, 1991
- A gene from the region of the human X inactivation centre is expressed exclusively from the inactive X chromosomeNature, 1991
- Erythroid colony growth from peripheral blood and bone marrow in polycythaemia.Journal of Clinical Pathology, 1990
- Cytogenetic Studies in Chronic Myeloproliferative DisordersActa Haematologica, 1983
- Cytogenetic studies on primary thrombocythaemiaHereditas, 1982