Unraveling the complex phenotype of dual diagnosis - Cerebellofaciodental syndrome and RELN-related lissencephaly

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dc.contributor.authorEsener, Zeynep
dc.contributor.authorOzgun, Nezir
dc.contributor.authorYaramis, Ahmet
dc.date.accessioned2025-07-03T21:27:11Z
dc.date.issued2024
dc.departmentBalıkesir Üniversitesi
dc.description.abstract[No abstract available]
dc.identifier.endpage1122
dc.identifier.issn1018-4813
dc.identifier.issn1476-5438
dc.identifier.scopusqualityQ1
dc.identifier.startpage1122
dc.identifier.urihttps://hdl.handle.net/20.500.12462/22092
dc.identifier.volume32
dc.identifier.wosWOS:001421430500889
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.language.isoen
dc.publisherSpringernature
dc.relation.ispartofEuropean Journal of Human Genetics
dc.relation.publicationcategoryKonferans Öğesi - Uluslararası - Kurum Öğretim Elemanı
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.snmzKA_WOS_20250703
dc.titleUnraveling the complex phenotype of dual diagnosis - Cerebellofaciodental syndrome and RELN-related lissencephaly
dc.typeConference Object

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