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The shift towards rare: Increased frequency of rare PGT-M cases

dc.contributor.authorOzer, Leyla
dc.contributor.authorUnsal, Evrim
dc.contributor.authorPolat, Merve
dc.contributor.authorAktuna, Suleyman
dc.contributor.authorBaltaci, Volkan
dc.date.accessioned2026-10-09T21:54:41Z
dc.date.issued2022
dc.departmentYüksek İhtisas Üniversitesi
dc.description.abstract[Abstract Not Available]
dc.identifier.endpage108
dc.identifier.issn1018-4813
dc.identifier.issn1476-5438
dc.identifier.issueSUPPL 1
dc.identifier.startpage108
dc.identifier.urihttps://hdl.handle.net/20.500.12794/4132
dc.identifier.volume30
dc.identifier.wosWOS:000779367700278
dc.identifier.wosqualityQ1
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynak.digerScience Citation Index Expanded (SCI-EXPANDED)
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_20260922
dc.subject[Keyword Not Available]
dc.titleThe shift towards rare: Increased frequency of rare PGT-M cases
dc.typeConference Object

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