Katalog der Deutschen Nationalbibliothek
Ergebnis der Suche nach: "DUMOULIN" and "Marie"
|
|
|
| Link zu diesem Datensatz | https://d-nb.info/1156200342 |
| Titel | HUWE1 variants cause dominant X-linked intellectual disability: a clinical study of 21 patients / by Stéphanie Moortgat, Siren Berland, Ingvild Aukrust, Isabelle Maystadt, Laura Baker, Valerie Benoit, Alfonso Caro-Llopis, Nicola S. Cooper, François-Guillaume Debray, Laurence Faivre, Thatjana Gardeitchik, Bjørn I. Haukanes, Gunnar Houge, Emma Kivuva, Francisco Martinez, Sarju G. Mehta, Marie-Cécile Nassogne, Nina Powell-Hamilton, Rolph Pfundt, Monica Rosello, Trine Prescott, Pradeep Vasudevan, Barbara van Loon, Christine Verellen-Dumoulin, Alain Verloes, Charlotte von der Lippe, Emma Wakeling, Andrew O. M. Wilkie, Louise Wilson, Amy Yuen, DDD Study, Karen J. Low, Ruth A. Newbury-Ecob |
| Person(en) |
Moortgat, Stéphanie (Verfasser) Berland, Siren (Sonstige) Aukrust, Ingvild (Sonstige) Maystadt, Isabelle (Sonstige) Baker, Laura (Sonstige) Benoit, Valerie (Sonstige) Caro-Llopis, Alfonso (Sonstige) Cooper, Nicola S. (Sonstige) Debray, François-Guillaume (Sonstige) Faivre, Laurence (Sonstige) Gardeitchik, Thatjana (Sonstige) Haukanes, Bjørn I. (Sonstige) Houge, Gunnar (Sonstige) Kivuva, Emma (Sonstige) Martinez, Francisco (Sonstige) Mehta, Sarju G. (Sonstige) Nassogne, Marie-Cécile (Sonstige) Powell-Hamilton, Nina (Sonstige) Pfundt, Rolph (Sonstige) Rosello, Monica (Sonstige) Prescott, Trine (Sonstige) Vasudevan, Pradeep (Sonstige) van Loon, Barbara (Sonstige) Verellen-Dumoulin, Christine (Sonstige) Verloes, Alain (Sonstige) Lippe, Charlotte von der (Sonstige) Wakeling, Emma (Sonstige) Wilkie, Andrew O. M. (Sonstige) Wilson, Louise (Sonstige) Yuen, Amy (Sonstige) Study, DDD (Sonstige) Low, Karen J. (Sonstige) Newbury-Ecob, Ruth A. (Sonstige) |
| Organisation(en) | SpringerLink (Online service) (Sonstige) |
| Umfang/Format | Online-Ressource : online resource. |
| Persistent Identifier |
URN: urn:nbn:de:1111-2018041617341 DOI: 10.1038/s41431-017-0038-6 |
| URL | http://dx.doi.org/10.1038/s41431-017-0038-6 (Open Access) |
| Zeitliche Einordnung | Erscheinungsdatum: 2017 |
| DDC-Notation | 616.04 (maschinell ermittelte DDC-Kurznotation) |
| Sprache(n) | Englisch (eng) |
| Beziehungen | Enthalten in: European journal of human genetics (Bd. 26, 27.11.2017, Nr. 1, date:1.2018: 64-74) |
| Sachgruppe(n) | 610 Medizin, Gesundheit |
| Online-Zugriff | Archivobjekt öffnen |

