Familial Platelet Disorder with Propensity to Myeloid Malignancy (FPDMM) Associated with Germline RUNX1 Mutation Shows Characteristic Morphologic Features

被引:0
|
作者
Kanagal-Shamanna, Rashmi [1 ]
Loghavi, Sanam [1 ]
Medeiros, L. Jeffrey [1 ]
Routbort, Mark J. [1 ]
Bueso-Ramos, Carlos E. [1 ]
Khoury, Joseph [1 ]
机构
[1] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
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暂无
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
1429
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页码:356A / 357A
页数:2
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