Exome-wide copy number variation analysis identifies a COL9A1 in frame deletion that is associated with hearing loss

Hofrichter, Michaela A. H.; Doll, Julia; Habibi, Haleh; Enayati, Samaneh; Mehrjardi, Mohammad Yahya Vahidi; Mueller, Tobias; Dittrich, Marcus; Haaf, Thomas; Vona, Barbara

dc.contributor.author	Vona, Barbara
dc.date.accessioned	2020-08-13T12:33:40Z
dc.date.available	2020-08-13T12:33:40Z
dc.date.issued	2019
dc.identifier.issn	1878-0849
dc.identifier.uri	http://hdl.handle.net/10900/104887
dc.language.iso	en	en
dc.publisher	Elsevier	de_DE
dc.relation.uri	http://dx.doi.org/10.1016/j.ejmg.2019.103724
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Exome-wide copy number variation analysis identifies a COL9A1 in frame deletion that is associated with hearing loss	de_DE
dc.type	Article	de_DE
utue.quellen.id	20200409032300_01306
utue.personen.roh	Hofrichter, Michaela A. H.
utue.personen.roh	Doll, Julia
utue.personen.roh	Habibi, Haleh
utue.personen.roh	Enayati, Samaneh
utue.personen.roh	Mehrjardi, Mohammad Yahya Vahidi
utue.personen.roh	Mueller, Tobias
utue.personen.roh	Dittrich, Marcus
utue.personen.roh	Haaf, Thomas
utue.personen.roh	Vona, Barbara
dcterms.isPartOf.ZSTitelID	European Journal of Medical Genetics	de_DE
dcterms.isPartOf.ZS-Issue	Article UNSP 103724	de_DE
dcterms.isPartOf.ZS-Volume	62	de_DE
utue.fakultaet	04 Medizinische Fakultät