Diagnosis and molecular characterization of a novel α0-thalassemia deletion (-Kozani) found in a Greek child with unexplained microcytic hypochromic anemia

被引：1
作者：
Makis, A. [1 ]
Georgiou, I. [2 ]
Traeger-Synodinos, J. [3 ]
Chaliasos, N. [1 ]
Grosso, M. [4 ]
Gambale, A. [4 ]
Iolascon, A. [4 ]
机构：
[1] Univ Ioannina, Dept Child Hlth, Fac Med, Ioannina, Greece
[2] Univ Ioannina, Dept Obstet & Gynecol, Genet & IVF Unit, Fac Med, Ioannina, Greece
[3] Natl & Kapodistrian Univ Athens, Med Genet Lab, Athens, Greece
[4] Univ Naples Federico II, Dept Mol Med & Med Biotechnol, CEINGE Adv Biotechnol, Naples, Italy
来源：
INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY | 2017年 / 39卷 / 05期
关键词：
THALASSEMIA; DISEASE;
D O I：
10.1111/ijlh.12690
中图分类号：
R5 [内科学];
学科分类号：
1002 ; 100201 ;
摘要：
引用
收藏
页码：E124 / E126
页数：3
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