Paris-Trousseau-type macrothrombocytopenia without 11q deletion

被引：0
|
作者：
Kaya, Zuhre [1 ]
Kocak, Ulker [1 ]
Percin, Ferda [2 ]
Kunishima, Shinji [4 ]
Albayrak, Meryem [1 ]
Gursel, Turkiz [1 ]
Ozogul, Candan [3 ]
机构：
[1] Gazi Univ, Sch Med, Dept Pediat, Pediat Hematol Unit, TR-06500 Ankara, Turkey
[2] Gazi Univ, Sch Med, Dept Clin Genet, TR-06500 Ankara, Turkey
[3] Gazi Univ, Sch Med, Dept Histol, TR-06500 Ankara, Turkey
[4] Natl Hosp Org Nagoya Med Ctr, Clin Res Ctr, Dept Hemostasis & Thrombosis, Nagoya, Aichi, Japan
来源：
PEDIATRICS INTERNATIONAL | 2010年 / 52卷 / 02期
关键词：
hereditary; macrothrombocytopenia; CLINICAL-FEATURES; JACOBSEN-SYNDROME; THROMBOCYTOPENIA; DYSMEGAKARYOPOIESIS; EXPRESSION; MUTATION; PATIENT; ANEMIA; CHILD;
D O I：
10.1111/j.1442-200X.2010.03043.x
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
[No abstract available]
引用
收藏
页码：e67 / e71
页数：5
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