dc.contributor.author |
Beck-Wödl, Stefanie |
|
dc.date.accessioned |
2021-05-10T06:44:41Z |
|
dc.date.available |
2021-05-10T06:44:41Z |
|
dc.date.issued |
2020 |
|
dc.identifier.issn |
1750-1172 |
|
dc.identifier.uri |
http://hdl.handle.net/10900/115136 |
|
dc.language.iso |
en |
de_DE |
dc.publisher |
Bmc |
de_DE |
dc.relation.uri |
http://dx.doi.org/10.1186/s13023-020-01557-8 |
de_DE |
dc.subject.ddc |
570 |
de_DE |
dc.subject.ddc |
610 |
de_DE |
dc.title |
The adult phenotype of Schaaf-Yang syndrome |
de_DE |
dc.type |
Article |
de_DE |
utue.quellen.id |
20210304112512_00994 |
|
utue.personen.roh |
Marbach, Felix |
|
utue.personen.roh |
Elgizouli, Magdeldin |
|
utue.personen.roh |
Rech, Megan |
|
utue.personen.roh |
Beygo, Jasmin |
|
utue.personen.roh |
Erger, Florian |
|
utue.personen.roh |
Velmans, Clara |
|
utue.personen.roh |
Stumpel, Constance T. R. M. |
|
utue.personen.roh |
Stegmann, Alexander P. A. |
|
utue.personen.roh |
Beck-Wodl, Stefanie |
|
utue.personen.roh |
Gillessen-Kaesbach, Gabriele |
|
utue.personen.roh |
Horsthemke, Bernhard |
|
utue.personen.roh |
Schaaf, Christian P. |
|
utue.personen.roh |
Kuechler, Alma |
|
dcterms.isPartOf.ZSTitelID |
Orphanet Journal of Rare Diseases |
de_DE |
dcterms.isPartOf.ZS-Issue |
Article 294 |
de_DE |
dcterms.isPartOf.ZS-Volume |
15 |
de_DE |
utue.fakultaet |
04 Medizinische Fakultät |
de_DE |