Craniofacial and Neurological Phenotype in a Patient with De Novo 18q Microdeletion and 18p Microduplication

被引：1
|
作者：
Yapijakis, Christos [1 ,2 ,3 ]
Angelopoulou, Antonia [2 ]
Manolakos, Emmanuel [4 ]
Voumvourakis, Costas [3 ]
机构：
[1] Natl & Kapodistrian Univ Athens, Haghia Sophia Hosp, Sch Med, Dept Pediat 1, Athens, Greece
[2] Cephalogenet Diagnost Ctr, Dept Mol Genet, Athens, Greece
[3] Natl & Kapodistrian Univ Athens, Attikon Hosp, Sch Med, Dept Neurol 2, Athens, Greece
[4] ATG Genet Ctr, Athens, Greece
来源：
GENEDIS 2018: GENETICS AND NEURODEGENERATION | 2020年 / 1195卷
关键词：
D O I：
10.1007/978-3-030-32633-3_22
中图分类号：
Q3 [遗传学];
学科分类号：
071007 ; 090102 ;
摘要：
引用
收藏
页码：163 / 166
页数：4
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