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P575: The Rare Genomes Project: Improving access to genomic sequencing and identifying causes of rare disease* |
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Titel: |
P575: The Rare Genomes Project: Improving access to genomic sequencing and identifying causes of rare disease* |
Auteur: |
Austin-Tse, Christina DiTroia, Stephanie O'Leary, Melanie VanNoy, Grace Mangilog, Brian Shah, Gulalai Martinez, Eva Serrano, Jillian Pais, Lynn O'Heir, Emily Osei-Owusu, Ikeoluwa Lemire, Gabrielle Ganesh, Vijay Stenton, Sarah Amin, Mutaz Socarras, Kayla Singh, Mugdha Hall, Stacey Larsson, Katie Singer-Berk, Moriel Marten, Daniel Wilson, Michael Snow, Hana Blankenmeister, Benjamin Ma, Jialan Weisburd, Ben Sanchis-Juan, Alba Brand, Harrison Groopman, Emily Lovgren, Alysia Williamson, Clara Hollyer, Marissa England, Eleina Seaby, Eleanor Chao, Katherine Goodrich, Julia Baxter, Samantha MacArthur, Daniel Talkowski, Michael Wojcik, Monica O'Donnell-Luria, Anne Rehm, Heidi |
Verschenen in: |
Genetics in medicine open |
Paginering: |
Jaargang 2 () nr. S1 pagina's p. |
Jaar: |
2024 |
Inhoud: |
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Uitgever: |
Published by Elsevier B.V. |
Bronbestand: |
Elektronische Wetenschappelijke Tijdschriften |
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