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 |
Article |
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 |