p11.2 CNVs detected by Array-CGH in a cohort of patients with intellectual disability, autism spectrum and obesity

被引：0
|
作者：
Carreira, I. M. [1 ,2 ,3 ]
Rosmaninho-Salgado, J. [4 ]
Pires, L. M. [1 ]
Saraiva, J. M. [4 ,5 ]
Sousa, S. B. [4 ,6 ]
Melo, J. B. [1 ,2 ,3 ]
机构：
[1] Univ Coimbra, Fac Med, Lab Citogenet & Genom, Coimbra, Portugal
[2] Univ Coimbra, Fac Med, CIMAGO, iCBR, Coimbra, Portugal
[3] Univ Coimbra, IBILI, CNC, Coimbra, Portugal
[4] Ctr Hosp & Univ Coimbra, Hosp Pediat, Serv Genet Med, Coimbra, Portugal
[5] Univ Coimbra, Fac Med, Clin Univ Pediat, Coimbra, Portugal
[6] Univ Coimbra, Fac Med, Inst Genet Med, Coimbra, Portugal
来源：
EUROPEAN JOURNAL OF HUMAN GENETICS | 2019年 / 27卷
关键词：
D O I：
暂无
中图分类号：
Q5 [生物化学]; Q7 [分子生物学];
学科分类号：
071010 ; 081704 ;
摘要：
E-P08.0516
引用
收藏
页码：942 / 943
页数：2
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