Acquired trisomy 21 and distinct clonal evolution in acute megakaryoblastic leukaemia in young monozygotic twins
Author:
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2002.03756.x/fullpdf
Reference12 articles.
1. Transplacental chemical exposure and risk of infant leukemia with MLL gene fusion;Alexander;Cancer Research,2001
2. Backtracking leukemia to birth: Identification of clonotypic gene fusion sequences in neonatal blood spots;Gale;Proceedings of the National Academy of Sciences of the United States of America,1997
3. Molecular genetics, natural history and the demise of childhood leukaemia;Greaves;European Journal of Cancer,1999
4. WorldHealth Organization classification of neoplastic diseasesofthe hematopoietic and lymphoid tissues: Report of theClinical Advisory Committee Meeting - Airlie House, Virginia,November 1997;Harris;Journal of Clinical Oncology,1999
5. Cryptic deletions and inversions of chromosome 21 in a phenotypically normal infant with transient abnormal myelopoiesis: a molecular cytogenetic study;Kempski;British Journal of Haematology,1998
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2. GATA1 mutation analysis and molecular landscape characterization in acute myeloid leukemia with trisomy 21 in pediatric patients;International Journal of Laboratory Hematology;2021-01-02
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4. DistinctGATA1Point Mutations in Monozygotic Twins With Down Syndrome and Transient Abnormal Myelopoiesis From a Triplet Pregnancy;American Journal of Clinical Pathology;2016-12
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