Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/22501
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dc.contributor.authorShukarova Angelovska, Elenaen_US
dc.contributor.authorAnastasovska, Violetaen_US
dc.contributor.authorDuma, Filipen_US
dc.contributor.authorMuaremovska, Ljeljaen_US
dc.contributor.authorNestoroska, Dragicaen_US
dc.contributor.authorIlieva, Gordanaen_US
dc.contributor.authorPesevska, Milicaen_US
dc.contributor.authorVelkov, Milanen_US
dc.date.accessioned2022-08-23T11:22:28Z-
dc.date.available2022-08-23T11:22:28Z-
dc.date.issued2020-06-06-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/22501-
dc.language.isoenen_US
dc.publisherSpringer Natureen_US
dc.relation.ispartofJournal of Human Geneticsen_US
dc.titleEarly onset of complex seizures as a first sign of 16p11.2 deletion syndromeen_US
dc.typeProceeding articleen_US
dc.relation.conference53th European Human Genetics Conference, Virtual. Berlin, Germany, June 6-9, 2020en_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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