Megakaryocyte hyperproliferation without GATA1 mutation in foetal liver of a case of Down syndrome with hydrops foetalis
- 24 September 2008
- journal article
- Published by Wiley in British Journal of Haematology
- Vol. 143 (2) , 300-303
- https://doi.org/10.1111/j.1365-2141.2008.07332.x
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Transcription factor GATA-1 and Down syndrome leukemogenesisLeukemia & Lymphoma, 2006
- The Proto-Oncogene ERG in Megakaryoblastic LeukemiasCancer Research, 2005
- Independent clones at separable stages of differentiation, bearing different GATA1 mutations, in the same TMD patient with Down syndromeBlood, 2005
- A Basic Classification and a Comprehensive Examination of Pediatric Myeloproliferative SyndromesJournal of Pediatric Hematology/Oncology, 2005
- Origins of leukaemia in children with Down syndromeNature Reviews Cancer, 2005
- Prenatal origin of GATA1 mutations may be an initiating step in the development of megakaryocytic leukemia in Down syndromeBlood, 2004
- Microarray transcript profiling distinguishes the transient from the acute type of megakaryoblastic leukaemia (M7) in Down's syndrome, revealing PRAME as a specific discriminating markerBritish Journal of Haematology, 2004
- Acquired mutations in GATA1 in neonates with Down's syndrome with transient myeloid disorderPublished by Elsevier ,2003
- Acquired mutations in GATA1 in the megakaryoblastic leukemia of Down syndromeNature Genetics, 2002
- Fetal hydrops and hepatosplenomegaly in the second half of pregnancy: a sign of myeloproliferative disorder in fetuses with trisomy 21Ultrasound in Obstetrics & Gynecology, 2001