Miller (GeneWiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH

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dc.contributor.author Riess, Angelika
dc.date.accessioned 2014-03-06T10:46:48Z
dc.date.available 2014-03-06T10:46:48Z
dc.date.issued 2012
dc.identifier.issn 0964-6906
dc.identifier.uri http://hdl.handle.net/10900/43023
dc.language.iso en de_DE
dc.publisher Oxford Univ Press de_DE
dc.relation.uri http://dx.doi.org/10.1093/hmg/dds218 de_DE
dc.rights info:eu-repo/semantics/closedAccess
dc.subject.ddc 570 de_DE
dc.subject.ddc 610 de_DE
dc.title Miller (GeneWiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH de_DE
dc.type Artikel de_DE
utue.quellen.id 20140226071329_01006 de_DE
utue.publikation.seiten 3969-3983 de_DE
utue.personen.roh Rainger, Joe
utue.personen.roh Bengani, Hemant
utue.personen.roh Campbell, Leigh
utue.personen.roh Anderson, Eve
utue.personen.roh Sokhi, Kishan
utue.personen.roh Lam, Wayne
utue.personen.roh Riess, Angelika
utue.personen.roh Ansari, Morad
utue.personen.roh Smithson, Sarah
utue.personen.roh Lees, Melissa
utue.personen.roh Mercer, Catherine
utue.personen.roh McKenzie, Kathryn
utue.personen.roh Lengfeld, Tobias
utue.personen.roh Gener Querol, Blanca
utue.personen.roh Branney, Peter
utue.personen.roh McKay, Stewart
utue.personen.roh Morrison, Harris
utue.personen.roh Medina, Bethan
utue.personen.roh Robertson, Morag
utue.personen.roh Kohlhase, Juergen
utue.personen.roh Gordon, Colin
utue.personen.roh Kirk, Jean
utue.personen.roh Wieczorek, Dagmar
utue.personen.roh FitzPatrick, David R.
dcterms.isPartOf.ZSTitelID Human Molecular Genetics de_DE
dcterms.isPartOf.ZS-Issue 18 de_DE
dcterms.isPartOf.ZS-Volume 21 de_DE
utue.fakultaet 04 Medizinische Fakultät de_DE


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