P679: Ultrarapid whole genome sequencing facilitates early definitive diagnosis of rare genetic disorders
oleh: Babi Ramesh Reddy Nallamilli, Jagannathan Lakshmanan, Vinish Ramachander, Supan Dhillon, Ruby Liu, Yinghong Pan, Naga Guruju, Christin Collins, Lora Bean, Madhuri Hegde
| Format: | Article |
|---|---|
| Diterbitkan: | Elsevier 2024-01-01 |
Deskripsi
No description available for this item.