Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12188/22356
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dc.contributor.authorNestoroska, Den_US
dc.contributor.authorAnastasovska, Ven_US
dc.contributor.authorShukarova Angelovska, Een_US
dc.contributor.authorPesevska, Men_US
dc.contributor.authorVeseli, Aen_US
dc.contributor.authorIlieva, Gen_US
dc.date.accessioned2022-08-16T11:18:24Z-
dc.date.available2022-08-16T11:18:24Z-
dc.date.issued2021-08-28-
dc.identifier.urihttp://hdl.handle.net/20.500.12188/22356-
dc.language.isoenen_US
dc.publisherSpringer Natureen_US
dc.relation.ispartofEuropean Journal of Human Geneticsen_US
dc.titleClinical and genomic characterization of 7q31.1 microduplication in a patient with developmental and neurological disabilitiesen_US
dc.typeProceeding articleen_US
dc.relation.conference54th European Society of Human Genetics (ESHG) Conference, Vienna -Austria, 28-31 August, 2021, P11.014.Den_US
item.fulltextWith Fulltext-
item.grantfulltextopen-
crisitem.author.deptFaculty of Medicine-
crisitem.author.deptFaculty of Medicine-
Appears in Collections:Faculty of Medicine: Journal Articles
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