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

页码：2728 / 2729

页数：2