A newborn infant with infantile spinal muscular atrophy associated with trisomy 21 and congenital hypothyroidism

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dc.authorwosidGürses, İclal/AAH-8552-2021
dc.contributor.authorGulcan, H
dc.contributor.authorUzum, I
dc.contributor.authorDayangac, D
dc.contributor.authorGurses, I
dc.date.accessioned2024-08-04T20:56:20Z
dc.date.available2024-08-04T20:56:20Z
dc.date.issued2005
dc.departmentİnönü Üniversitesien_US
dc.description.abstract[Abstract Not Available]en_US
dc.identifier.endpage114en_US
dc.identifier.issn1015-8146
dc.identifier.issue1en_US
dc.identifier.pmid15844790en_US
dc.identifier.startpage113en_US
dc.identifier.urihttps://hdl.handle.net/11616/102212
dc.identifier.volume16en_US
dc.identifier.wosWOS:000228152300018en_US
dc.identifier.wosqualityQ4en_US
dc.indekslendigikaynakWeb of Scienceen_US
dc.indekslendigikaynakPubMeden_US
dc.language.isoenen_US
dc.publisherMedecine Et Hygieneen_US
dc.relation.ispartofGenetic Counselingen_US
dc.relation.publicationcategoryDiğeren_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectThyroid-Dysfunctionen_US
dc.subjectDowns-Syndromeen_US
dc.subjectChildrenen_US
dc.titleA newborn infant with infantile spinal muscular atrophy associated with trisomy 21 and congenital hypothyroidismen_US
dc.typeLetteren_US

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