BCL11B-related disease: a single phenotypic entity?

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dc.contributor.authorVedovato\\-dos\\-Santos, Juliana Heather
dc.contributor.authorTooze, Rebecca
dc.contributor.authorMccann, Emma
dc.contributor.authorSithambaram, Sivagamy
dc.contributor.authorAlanay, Yasemin
dc.contributor.authorJohnson, David
dc.contributor.authorDogan, Ozlem Akgun
dc.contributor.authorKilercik, Meltem
dc.contributor.authorBingol, Aysen
dc.contributor.authorOzek, Memet
dc.contributor.authorNellaker, Christoffer
dc.contributor.authorTwigg, Stephen
dc.contributor.authorWilkie, Andrew
dc.date.accessioned2025-10-16T15:12:21Z
dc.date.issued2024
dc.description.abstract57th Conference of the European-Society-of-Human-Genetics (ESHG), Berlin, GERMANY, JUN 01-04, 2024
dc.identifier.otherWOS:001407868902444
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/5390
dc.publisherSPRINGERNATURE
dc.sourceEUROPEAN JOURNAL OF HUMAN GENETICS
dc.titleBCL11B-related disease: a single phenotypic entity?
dc.typeMeeting Abstract

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