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p53 mutation as the second event in juvenile chronic myelogenous leukemia in a patient with neurofibromatosis type 1

โœ Scribed by Drorit Luria; Smadar Avigad; Ian J. Cohen; Batia Stark; Raphael Weitz; Rina Zaizov


Publisher
John Wiley and Sons
Year
1997
Tongue
English
Weight
159 KB
Volume
80
Category
Article
ISSN
0008-543X

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โœฆ Synopsis


risk of developing various malignancies, most of which are myeloid disorders. The observed loss of NF1 allele in the myeloid malignancies of NF1 patients suggests


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