Mutation profiling in South African patients with Cornelia de Lange syndrome phenotype

dc.article.end-page6en
dc.article.start-page1en
dc.citation.doi10.1002/MGG3.2342en
dc.contributor.authorHeather Seymouren
dc.contributor.authorCandice Febenen
dc.contributor.authorPatracia Nevondween
dc.contributor.authorRobyn Kerren
dc.contributor.authorC Spenceren
dc.contributor.authorMabyalwa Mudauen
dc.contributor.authorE Honeyen
dc.contributor.authorZane Lombarden
dc.contributor.authorAmanda Krauseen
dc.contributor.authorNadia Carstensen
dc.date.accessioned2024-10-11T14:13:38Z
dc.date.available2024-10-11T14:13:38Z
dc.facultyFACULTY OF HEALTH SCIENCESen
dc.identifier.citationWOSen
dc.identifier.issn0891-4168en
dc.identifier.urihttps://hdl.handle.net/10539/41499
dc.journal.titleMutation profiling in South African patients with Cornelia de Lange syndrome phenotypeen
dc.journal.volume12en
dc.titleMutation profiling in South African patients with Cornelia de Lange syndrome phenotypeen
dc.typeJournal Articleen
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