Interstitial 1p32.1p32.3 deletion in a patient with multiple congenital anomalies

Kehrer, Martin; Schaeferhoff, Karin; Bonin, Michael; Jauch, Anna; Bevot, Andrea; Tzschach, Andreas

dc.contributor.author	Kehrer, Martin
dc.contributor.author	Bonin, Michael
dc.contributor.author	Bevot, Andrea
dc.contributor.author	Tzschach, Andreas
dc.contributor.author	Schäferhoff, Karin
dc.date.accessioned	2016-01-14T09:14:21Z
dc.date.available	2016-01-14T09:14:21Z
dc.date.issued	2015
dc.identifier.issn	1552-4825
dc.identifier.uri	http://hdl.handle.net/10900/67610
dc.language.iso	en	en
dc.publisher	Wiley - Blackwell	de_DE
dc.relation.uri	http://dx.doi.org/10.1002/ajmg.a.37178	de_DE
dc.rights	info:eu-repo/semantics/closedAccess
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Interstitial 1p32.1p32.3 deletion in a patient with multiple congenital anomalies	de_DE
dc.type	Article	de_DE
utue.quellen.id	20151209042647_00466
utue.publikation.seiten	2406-2410	de_DE
utue.personen.roh	Kehrer, Martin
utue.personen.roh	Schaeferhoff, Karin
utue.personen.roh	Bonin, Michael
utue.personen.roh	Jauch, Anna
utue.personen.roh	Bevot, Andrea
utue.personen.roh	Tzschach, Andreas
dcterms.isPartOf.ZSTitelID	American Journal of Medical Genetics Part A	de_DE
dcterms.isPartOf.ZS-Issue	10	de_DE
dcterms.isPartOf.ZS-Volume	167	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE