Baraitser-Winter Syndrome in a boy with heterozygous missense mutation in the ACTB gene

dc.contributor.authorTemel, S. G.
dc.contributor.authorEkmekci, G.
dc.contributor.authorYenmis, G.
dc.contributor.authorKiper, P. O. Simsek
dc.contributor.authorAlanay, Y.
dc.date.accessioned2025-10-16T15:25:05Z
dc.date.issued2018
dc.description.abstract50th European-Society-of-Human-Genetics (ESHG) Conference, Copenhagen, DENMARK, MAY 27-30, 2017
dc.identifier.otherWOS:000489312608068
dc.identifier.urihttps://openaccess.acibadem.edu.tr/handle/11443/8202
dc.publisherNATURE PUBLISHING GROUP
dc.sourceEUROPEAN JOURNAL OF HUMAN GENETICS
dc.titleBaraitser-Winter Syndrome in a boy with heterozygous missense mutation in the ACTB gene
dc.typeMeeting Abstract

Dosyalar

Koleksiyonlar