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A novel RUNX1 mutation in a kindred with familial platelet disorder with propensity to acute myeloid leukaemia: male predominance of affected individuals

✍ Scribed by Stephen E. Langabeer; Carolyn J. Owen; Sarah L. McCarron; Jude Fitzgibbon; Owen P. Smith; Aengus O’Marcaigh; Paul Browne


Book ID
114794836
Publisher
John Wiley and Sons
Year
2010
Tongue
English
Weight
90 KB
Volume
85
Category
Article
ISSN
0902-4441

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