Supernumerary chromosome der(22)t(11;22): Emanuel Syndrome association with novel features

dc.contributor.author	KURU, RAHIYE DILHAN
dc.contributor.author	YILMAZ, ŞÜKRİYE
dc.contributor.author	TARKAN ARGÜDEN, YELDA
dc.contributor.author	ÇIRAKOĞLU, AYŞE
dc.contributor.author	YOSUNKAYA, ELİF
dc.contributor.author	Hacıhanefioğlu, Seniha
dc.contributor.author	DEVİREN, AYHAN
dc.contributor.author	SAĞCI GÜVEN, GÜLGÜN
dc.date.accessioned	2021-03-05T11:41:38Z
dc.date.available	2021-03-05T11:41:38Z
dc.date.issued	2007
dc.identifier.citation	YOSUNKAYA E., SAĞCI GÜVEN G., KURU R. D. , YILMAZ Ş., TARKAN ARGÜDEN Y., ÇIRAKOĞLU A., DEVİREN A., Hacıhanefioğlu S., "Supernumerary chromosome der(22)t(11;22): Emanuel Syndrome association with novel features", GENETIC COUNSELING, cilt.18, ss.401-408, 2007
dc.identifier.issn	1015-8146
dc.identifier.other	vv_1032021
dc.identifier.other	av_a9656380-4499-48c0-8d80-5f6415aac8fb
dc.identifier.uri	http://hdl.handle.net/20.500.12627/113155
dc.language.iso	eng
dc.subject	Sağlık Bilimleri
dc.subject	Klinik Tıp (MED)
dc.subject	Tıp
dc.title	Supernumerary chromosome der(22)t(11;22): Emanuel Syndrome association with novel features
dc.type	Makale
dc.relation.journal	GENETIC COUNSELING
dc.contributor.department	İstanbul Üniversitesi , ,
dc.identifier.volume	18
dc.identifier.issue	4
dc.identifier.startpage	401
dc.identifier.endpage	408
dc.contributor.firstauthorID	598425

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