The clinical phenotype of Koolen-de Vries syndrome in Turkish patients and literature review

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dc.contributor.authorKaramik, Gokcen
dc.contributor.authorTuysuz, Beyhan
dc.contributor.authorIsik, Esra
dc.contributor.authorYilmaz, Aysegul
dc.contributor.authorAlanay, Yasemin
dc.contributor.authorSunamak, Evrim Cifci
dc.contributor.authorDurmusalioglu, Enise Avci
dc.contributor.authorOzkinay, Ferda
dc.contributor.authorCetin, Gokhan Ozan
dc.contributor.authorOzturk, Nuray
dc.contributor.authorMihci, Ercan
dc.contributor.authorNur, Banu
dc.date.accessioned2025-10-16T15:15:35Z
dc.date.issued2023
dc.identifier.doi10.1002/ajmg.a.63207
dc.identifier.otherWOS:000970974600001
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/6483
dc.publisherWILEY
dc.sourceAMERICAN JOURNAL OF MEDICAL GENETICS PART A
dc.subject17q21
dc.subject31 microdeletion syndrome
dc.subjectKdVS
dc.subjectKoolen\\-de Vries syndrome
dc.subjectmolecular karyotyping
dc.titleThe clinical phenotype of Koolen-de Vries syndrome in Turkish patients and literature review
dc.typeReview

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