First African case report of hypoparathyroidism deafness and renal dysplasia HDR syndrome due to inverted duplication and deletion of chromosome 10p

Simple item page
dc.article.end-page7en
dc.article.start-page1en
dc.citation.doi10.1186/S43042-024-00619-Xen
dc.contributor.authorT Sathekgeen
dc.contributor.authorG Rikhotsoen
dc.contributor.authorBianca Rossouwen
dc.contributor.authorBronwyn Dillonen
dc.contributor.authorFiona Baine-Savanhuen
dc.date.accessioned2026-04-18T21:45:46Z
dc.facultyFACULTY OF HEALTH SCIENCESen
dc.identifier.citationWOSen
dc.identifier.issn1110-8630en
dc.identifier.urihttps://hdl.handle.net/10539/49062
dc.journal.titleFirst African case report of hypoparathyroidism deafness and renal dysplasia HDR syndrome due to inverted duplication and deletion of chromosome 10pen
dc.journal.volume25en
dc.titleFirst African case report of hypoparathyroidism deafness and renal dysplasia HDR syndrome due to inverted duplication and deletion of chromosome 10pen
dc.typeJournal Articleen

Files

Original bundle

Now showing 1 - 1 of 1
Thumbnail Image
Name:
Journal Article.pdf
Size:
901.54 KB
Format:
Adobe Portable Document Format
Description:
Bitstream uploaded by REST Client
Download

Collections

Academic Wits Research Outputs (All submissions)