P679: Ultrarapid whole genome sequencing facilitates early definitive diagnosis of rare genetic disorders
| Autor: | Nallamilli, Babi Ramesh Reddy, Lakshmanan, Jagannathan, Ramachander, Vinish, Dhillon, Supan, Liu, Ruby, Pan, Yinghong, Guruju, Naga, Collins, Christin, Bean, Lora, Hegde, Madhuri |
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| Zdroj: | In Genetics in Medicine Open 2024 2 Supplement 1 |
| Databáze: | ScienceDirect |
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