 | Up a level |
2021
Khanam, Tasneem, Sandmann, Sarah 
ORCID: 0000-0002-5011-0641, Seggewiss, Jochen, Ruether, Charlotte, Zimmermann, Martin, Norvil, Allison B., Bartenhagen, Christoph, Randau, Gerrit, Mueller, Stephanie, Herbrueggen, Heidi, Hoffmann, Per, Herms, Stefan, Wei, Lanying, Woeste, Marius, Wuensch, Christian, Gowher, Humaira, Oschlies, Ilske, Klapper, Wolfram, Woessmann, Wilhelm, Dugas, Martin and Burkhardt, Birgit ORCID: 0000-0002-1151-829X
(2021).
Integrative genomic analysis of pediatric T-cell lymphoblastic lymphoma reveals candidates of clinical significance.
Blood, 137 (17).
S. 2347 - 2360.
WASHINGTON:
AMER SOC HEMATOLOGY.
ISSN 1528-0020
2019
Wallmeier, Julia, Frank, Diana, Shoemark, Amelia, Noethe-Menchen, Tabea, Cindric, Sandra, Olbrich, Heike, Loges, Niki T., Aprea, Isabella, Dougherty, Gerard W., Pennekamp, Petra, Kaiser, Thomas ORCID: 0000-0002-6699-0014, Mitchison, Hannah M., Hogg, Claire, Carr, Siobhan B., Zariwala, Maimoona A., Ferkol, Thomas, Leigh, Margaret W., Davis, Stephanie D., Atkinson, Jeffrey, Dutcher, Susan K., Knowles, Michael R., Thiele, Holger, Altmueller, Janine, Krenz, Henrike, Woeste, Marius, Brentrup, Angela, Ahrens, Frank, Vogelberg, Christian, Morris-Rosendahl, Deborah J. and Omran, Heymut
(2019).
De Novo Mutations in FOXJ1 Result in a Motile Ciliopathy with Hydrocephalus and Randomization of Left/Right Body Asymmetry.
Am. J. Hum. Genet., 105 (5).
S. 1030 - 1040.
CAMBRIDGE:
CELL PRESS.
ISSN 1537-6605