Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/22353
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dc.contributor.authorAnastasovska, Violetaen_US
dc.contributor.authorShukarova Angelovska, Elenaen_US
dc.contributor.authorNestoroska, Dragicaen_US
dc.contributor.authorZdraveska, Nikolinaen_US
dc.contributor.authorIlieva, Gordanaen_US
dc.contributor.authorPesevska, Milicaen_US
dc.contributor.authorStojanova, Ivanaen_US
dc.date.accessioned2022-08-16T11:11:15Z-
dc.date.available2022-08-16T11:11:15Z-
dc.date.issued2021-08-28-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/22353-
dc.language.isoenen_US
dc.relation.ispartofEuropean Journal of Human Geneticsen_US
dc.titleDetection of 3p25 microdeletion syndrome in the Macedonian patient with significant psychomotor retardationen_US
dc.typeProceeding articleen_US
dc.relation.conference54th European Society of Human Genetics Conference (ESHG), 28-31 August, 2021, P11.046.Den_US
item.fulltextWith Fulltext-
item.grantfulltextopen-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Conference papers
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