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
来源：
LABORATORY INVESTIGATION | 2017年 / 97卷
关键词：
D O I：
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
引用
收藏
页码：356A / 357A
页数：2
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