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1 例 17q12 微缺失综合征合并听力缺陷的患儿 及其父母基因检测结果分析.

Authors :
庄晨露
李承燕
刘玲
谢造业
马歆静
叶中绿
Source :
Shandong Medical Journal; 10/25/2024, Vol. 64 Issue 30, p70-72, 3p
Publication Year :
2024

Abstract

<i>Copyright of Shandong Medical Journal is the property of Shandong Medical Health Newspapers and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)

Details

Language :
Chinese
ISSN :
1002266X
Volume :
64
Issue :
30
Database :
Complementary Index
Journal :
Shandong Medical Journal
Publication Type :
Academic Journal
Accession number :
181238113
Full Text :
https://doi.org/10.3969/j.issn.1002-266X.2024.30.016