Exploring the benefits, harms, and costs of genomic newborn screening for rare diseases
| Main Authors: | , , , , , , , , , |
|---|---|
| Format: | Journal article |
| Language: | English |
| Published: |
Springer Nature
2024
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| _version_ | 1811140535618895872 |
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| author | Baple, EL Scott, RH Banka, S Buchanan, J Fish, L Wynn, S Wilkinson, J Ellard, S MacArthur, DG Stark, Z |
| author_facet | Baple, EL Scott, RH Banka, S Buchanan, J Fish, L Wynn, S Wilkinson, J Ellard, S MacArthur, DG Stark, Z |
| author_sort | Baple, EL |
| collection | OXFORD |
| description | |
| first_indexed | 2024-09-25T04:23:32Z |
| format | Journal article |
| id | oxford-uuid:5fb5b046-e08b-4cd8-8488-a2de73d76517 |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-09-25T04:23:32Z |
| publishDate | 2024 |
| publisher | Springer Nature |
| record_format | dspace |
| spelling | oxford-uuid:5fb5b046-e08b-4cd8-8488-a2de73d765172024-08-21T13:49:50ZExploring the benefits, harms, and costs of genomic newborn screening for rare diseasesJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:5fb5b046-e08b-4cd8-8488-a2de73d76517EnglishSymplectic ElementsSpringer Nature2024Baple, ELScott, RHBanka, SBuchanan, JFish, LWynn, SWilkinson, JEllard, SMacArthur, DGStark, Z |
| spellingShingle | Baple, EL Scott, RH Banka, S Buchanan, J Fish, L Wynn, S Wilkinson, J Ellard, S MacArthur, DG Stark, Z Exploring the benefits, harms, and costs of genomic newborn screening for rare diseases |
| title | Exploring the benefits, harms, and costs of genomic newborn screening for rare diseases |
| title_full | Exploring the benefits, harms, and costs of genomic newborn screening for rare diseases |
| title_fullStr | Exploring the benefits, harms, and costs of genomic newborn screening for rare diseases |
| title_full_unstemmed | Exploring the benefits, harms, and costs of genomic newborn screening for rare diseases |
| title_short | Exploring the benefits, harms, and costs of genomic newborn screening for rare diseases |
| title_sort | exploring the benefits harms and costs of genomic newborn screening for rare diseases |
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