The implementation and utility of clinical exome sequencing in a South African infant cohort

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dc.article.end-page13en
dc.article.start-page1en
dc.citation.doi10.3389/FGENE.2023.1277948en
dc.contributor.authorLisa Campbellen
dc.contributor.authorJoy Fredericksen
dc.contributor.authorKhakhu Mathivhaen
dc.contributor.authorPalesa Mosheshen
dc.contributor.authorAshraf Coovadiaen
dc.contributor.authorP Chirwaen
dc.contributor.authorBronwyn Dillonen
dc.contributor.authorAzra Ghooren
dc.contributor.authorDelania Lawrenceen
dc.contributor.authorLoshnee Nairen
dc.contributor.authorNjabulo Mabasoen
dc.contributor.authorDaisy Mokweleen
dc.contributor.authorMichael Novellieen
dc.contributor.authorAmanda Krauseen
dc.contributor.authorNadia Carstensen
dc.date.accessioned2024-07-23T06:01:36Z
dc.date.available2024-07-23T06:01:36Z
dc.departmentHUMAN GENETICSen
dc.facultyFACULTY OF HEALTH SCIENCESen
dc.identifier.citationWOSen
dc.identifier.urihttps://hdl.handle.net/10539/39682
dc.journal.titleThe implementation and utility of clinical exome sequencing in a South African infant cohorten
dc.journal.volume14en
dc.titleThe implementation and utility of clinical exome sequencing in a South African infant cohorten
dc.typeJournal Articleen
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