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

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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 Artikel 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


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