| 标题 |
A first large study of whole-exome sequencing (WES) in 489 patients with suspected rare genetic disorders at a tertiary centre in Malaysia |
| 网址 | |
| DOI | |
| 其它 |
期刊:Rare 作者:Lip Hen Moey; Go Hun Seo; Boon Eu Cheah; Wee Teik Keng; Hane Lee; et al 出版日期:2025-07-19 |
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(2025-6-4)