Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556

dc.contributor.author	Koko, Mahmoud
dc.date.accessioned	2020-05-04T11:31:05Z
dc.date.available	2020-05-04T11:31:05Z
dc.date.issued	2019
dc.identifier.issn	1364-6753
dc.identifier.uri	http://hdl.handle.net/10900/100211
dc.language.iso	en	de_DE
dc.publisher	Springer	de_DE
dc.relation.uri	http://dx.doi.org/10.1007/s10048-019-00577-2	de_DE
dc.subject.ddc	570	de_DE
dc.subject.ddc	610	de_DE
dc.title	Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556	de_DE
dc.type	Article	de_DE
utue.quellen.id	20190926111821_01582
utue.publikation.seiten	91-98	de_DE
utue.personen.roh	Cauley, Edmund S.
utue.personen.roh	Hamed, Ahlam
utue.personen.roh	Mohamed, Inaam N.
utue.personen.roh	Elseed, Maha
utue.personen.roh	Martinez, Samantha
utue.personen.roh	Yahia, Ashraf
utue.personen.roh	Abozar, Fatima
utue.personen.roh	Abubakr, Rayan
utue.personen.roh	Koko, Mahmoud
utue.personen.roh	Elsayed, Liena
utue.personen.roh	Piao, Xianhua
utue.personen.roh	Salih, Mustafa A.
utue.personen.roh	Manzini, M. Chiara
dcterms.isPartOf.ZSTitelID	Neurogenetics	de_DE
dcterms.isPartOf.ZS-Issue	2	de_DE
dcterms.isPartOf.ZS-Volume	20	de_DE
utue.fakultaet	04 Medizinische Fakultät	de_DE

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