Prenatal origin of GATA1 mutations may be an initiating step in the development of megakaryocytic leukemia in Down syndrome
- 1 September 2004
- journal article
- Published by American Society of Hematology in Blood
- Vol. 104 (5), 1588-1589
- https://doi.org/10.1182/blood-2004-04-1563
Abstract
No abstract availableKeywords
This publication has 9 references indexed in Scilit:
- Natural history of GATA1 mutations in Down syndromeBlood, 2004
- Recent insights into the mechanisms of myeloid leukemogenesis in Down syndromeBlood, 2004
- Fetal origin of the GATA1 mutation in identical twins with transient myeloproliferative disorder and acute megakaryoblastic leukemia accompanying Down syndromeBlood, 2004
- Transient leukaemia – a benign form of leukaemia in newborn infants with trisomy 21British Journal of Haematology, 2003
- Acquired mutations in GATA1 in the megakaryoblastic leukemia of Down syndromeNature Genetics, 2002
- Homocysteine Metabolism in Children with Down Syndrome: In Vitro ModulationAmerican Journal of Human Genetics, 2001
- Atypical background somatic mutant frequencies at the HPRT locus in children and adults with Down syndromeMutation Research, 1998
- Identification and Tissue Distribution of Human Cystathionine β-Synthase mRNA IsoformsArchives of Biochemistry and Biophysics, 1998
- Unusual diffuse liver fibrosis accompanying transient myeloproliferative disorder in Down's syndrome: a report of four autopsy cases and proposal of a hypothesisBlood, 1992