Marked genetic heterogeneity in familial myelodysplasia/acute myeloid leukaemia
Author:
Affiliation:
1. Barts and the London School of Medicine and Dentistry; Queen Mary University of London; Barts and The London Children's Hospital; London UK
Funder
Wellcome Trust
Publisher
Wiley
Subject
Hematology
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.2012.09136.x/fullpdf
Reference19 articles.
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2. Germ-line GATA2 p.THR354MET mutation in familial myelodysplastic syndrome with acquired monosomy 7 and ASXL1 mutation demonstrating rapid onset and poor survival;Bodor;Haematologica,2012
3. Detection of an interstitial 3q21.1-q21.3 deletion in a child with multiple congenital abnormalities, mental retardation, pancytopenia, and myelodysplasia;Callier;American Journal of Medical Genetics. Part A,2009
4. Mutation in TET2 in myeloid cancers;Delhommeau;The New England Journal of Medicine,2009
5. Exome sequencing identifies GATA-2 mutation as the cause of dendritic cell, monocyte, B and NK lymphoid deficiency;Dickinson;Blood,2011
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