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P679: Ultrarapid whole genome sequencing facilitates early definitive diagnosis of rare genetic disorders |
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Titel: |
P679: Ultrarapid whole genome sequencing facilitates early definitive diagnosis of rare genetic disorders |
Auteur: |
Nallamilli, Babi Ramesh Reddy Lakshmanan, Jagannathan Ramachander, Vinish Dhillon, Supan Liu, Ruby Pan, Yinghong Guruju, Naga Collins, Christin Bean, Lora Hegde, Madhuri |
Verschenen in: |
Genetics in medicine open |
Paginering: |
Jaargang 2 () nr. S1 pagina's p. |
Jaar: |
2024 |
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Uitgever: |
Published by Elsevier B.V. |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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