Phenotypic and genetic study of a child with deletion of chromosome 2q and obstructive sleep apnea syndrome and deafness

被引：0
|
作者：
Xu, Ying [1 ]
Jiang, Lan [1 ]
Zhao, Jing [2 ]
Han, Fugen [1 ,3 ]
机构：
[1] Zhengzhou Childrens Hosp, Henan Childrens Hosp, Dept Otorhinolaryngol Head & Neck Surg, Zhengzhou 450003, Peoples R China
[2] Capital Med Univ, Beijing Childrens Hosp, Natl Ctr Childrens Hlth, Dept Otolaryngol Head & Neck Surg, Beijing 100045, Peoples R China
[3] Zhengzhou Childrens Hosp, Henan Childrens Hosp, Dept Otorhinolaryngol Head & Neck Surg, 33 Eastern Outer Loop Dragon Lake, Zhengzhou 450003, Peoples R China
来源：
ASIAN JOURNAL OF SURGERY | 2023年 / 46卷 / 07期
关键词：
2q12.1q14.1; deletion; Congenital hypothyroidism; Congenital deafness; Mental retardation; Developmental delay; CNV-seq;
D O I：
10.1016/j.asjsur.2023.01.031
中图分类号：
R61 [外科手术学];
学科分类号：
摘要：
引用
收藏
页码：2728 / 2729
页数：2
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