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

页码：356A / 357A

页数：2

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