De-novo interstitial 2.33Mb deletion in 8q24.3: new insights on a very rare partial monosomy syndrome

被引：3

作者：

Akbaroghli, Susan ^{[1
,3
]}

Tonekaboni, Seyed H. ^{[2
,3
]}

Kariminejad, Roxana ^{[4
]}

Liehr, Thomas ^{[5
]}

Coci, Emanuele G. ^{[6
,7
]}

机构：

[1] Shahid Beheshti Univ Med Sci, Mofid Childrens Hosp, Div Clin Genet, Dept Pediat, Tehran, Iran

[2] Shahid Beheshti Univ Med Sci, Mofid Childrens Hosp, Child Neurol Dept, Tehran, Iran

[3] Shahid Beheshti Univ Med Sci, Mofid Childrens Hosp, Pediat Neurol Res Ctr, Tehran, Iran

[4] Kariminejad Najmabadi Pathol & Genet Ctr, Tehran, Iran

[5] Jena Univ Hosp, Inst Human Genet, Jena, Germany

[6] Pediat Clin, Dept Pediat Neurol, Braunschweig, Germany

[7] Ruhr Univ Bochum, Univ Childrens Hosp, Dept Neuropediat, Bochum, Germany

来源：

CLINICAL DYSMORPHOLOGY | 2018年 / 27卷 / 03期

关键词：

GENE;

D O I：

10.1097/MCD.0000000000000224

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

[No abstract available]

引用

页码：97 / 100

页数：4

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