Severe congenital neutropenia in two siblings related to HAX1 mutation without neurodevelopmental disorders

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dc.contributor.authorPATIROĞLU TÜRKAN
dc.contributor.authorEKE GUNGOR HATICE
dc.contributor.authorTRIOT ALEXO
dc.contributor.authorÜNAL EKREM
dc.contributor.authorÜnal, Ekrem
dc.date.accessioned2026-06-12T11:49:31Z
dc.date.issued2013
dc.descriptionSCI-Expanded | YÖK-Özgeçmiş
dc.identifier.issn1015-8146
dc.identifier.urihttps://hdl.handle.net/20.500.11782/6028
dc.relation.ispartofGENETIC COUNSELING
dc.titleSevere congenital neutropenia in two siblings related to HAX1 mutation without neurodevelopmental disorders
dspace.entity.typePublication
relation.isAuthorOfPublicationcd35ec05-b9b3-4f63-a13f-bc9dc6344971
relation.isAuthorOfPublication.latestForDiscoverycd35ec05-b9b3-4f63-a13f-bc9dc6344971

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