| 标题 |
Refining the clinical phenotype associated with missense variants in exons 38 and 39 of KMT2D |
| 网址 | |
| DOI | |
| 其它 |
期刊:American journal of medical genetics. Part A 作者:Tharreau M; Garde A; Marlin S; Morel G; Ernest S; et al 出版日期:2022/05/01 |
| 求助人 | |
| 下载 |
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(2025-6-4)