Deletion of the paternal allele of the imprinted MEST/PEG1 region in a patient with Silver-Russell syndrome features

Eggermann, T; Spengler, S.; Begemann, M.; Binder, Gerhard; Buiting, K.; Albrecht, B.; Spranger, S.

dc.contributor.author	Binder, Gerhard
dc.date.accessioned	2015-06-16T12:23:07Z
dc.date.available	2015-06-16T12:23:07Z
dc.date.issued	2012
dc.identifier.issn	0009-9163
dc.identifier.uri	http://hdl.handle.net/10900/63649
dc.language.iso	en	de_DE
dc.publisher	Oxford : Wiley-Blackwell	de_DE
dc.relation.uri	http://dx.doi.org/10.1111/j.1399-0004.2011.01719.x	de_DE
dc.rights	info:eu-repo/semantics/closedAccess
dc.subject.ddc	610	de_DE
dc.title	Deletion of the paternal allele of the imprinted MEST/PEG1 region in a patient with Silver-Russell syndrome features	de_DE
dc.type	Article	de_DE
utue.publikation.seiten	298-300	de_DE
utue.personen.roh	Eggermann, T
utue.personen.roh	Spengler, S.
utue.personen.roh	Begemann, M.
utue.personen.roh	Binder, Gerhard
utue.personen.roh	Buiting, K.
utue.personen.roh	Albrecht, B.
utue.personen.roh	Spranger, S.
dcterms.isPartOf.ZSTitelID	Clinical genetics	de_DE
dcterms.isPartOf.ZS-Issue	3	de_DE
dcterms.isPartOf.ZS-Volume	81	de_DE