Yayın: Investigation of genetic causation underlying microlissencephaly spectrum of disorders
| dc.contributor.advisor | supervisor Kaya Bilgüvar | |
| dc.contributor.author | Aral, Melisa | |
| dc.date.accessioned | 2026-07-13T06:52:13Z | |
| dc.date.issued | 2025-01-01 | |
| dc.department | Department of Genome Studies | |
| dc.format.extent | 84 s. tbl. | |
| dc.identifier.uri | https://openaccess.acibadem.edu.tr/handle/11443/10170 | |
| dc.institution | Institute Of Health Sciences | |
| dc.language.iso | en | |
| dc.publisher | Acıbadem Mehmet Ali Aydınlar Üniversitesi | |
| dc.subject | Microlissencephaly | |
| dc.subject | Neurodevelopmental disorders | |
| dc.subject | Rare diseases | |
| dc.subject | Variant interpretation | |
| dc.subject | Whole-exome sequencing | |
| dc.title | Investigation of genetic causation underlying microlissencephaly spectrum of disorders | |
| dc.type | masterthesis | |
| dspace.entity.type | Publication |
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