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Eine Ebene nach oben |
Gruppiert nach: Dokumententyp |
Veröffentlichungsdatum
Anzahl der Publikationen: 2
2018
Boutboul, David; Kuehn, Hye Sun; Wyngaert, Zoe van de; Niemela, Julie E.; Callebaut, Isabelle; Stoddard, Jennifer; Lenoir, Christelle; Barlogis, Vincent; Farnarier, Catherine; Vely, Frederic; Yoshida, Nao; Kojima, Seiji; Kanegane, Hirokazu; Hoshino, Akihiro; Hauck, Fabian; Lhermitte, Ludovic; Asnafi, Vahid; Roehrs, Philip; Chen, Shaoying; Verbsky, James W.; Calvo, Katherine R.; Husami, Ammar; Zhang, Kejian; Roberts, Joseph; Amrol, David; Sleaseman, John; Hsu, Amy P.; Holland, Steven M.; Marsh, Rebecca; Fischer, Alain; Fleisher, Thomas A.; Picard, Capucine; Latour, Sylvain und Rosenzweig, Sergio D.
(2018):
Dominant-negative IKZF1 mutations cause a T, B, and myeloid cell combined immunodeficiency.
In: Journal of Clinical Investigation, Bd. 128, Nr. 7: S. 3071-3087
2016
Hartz, Bernd; Marsh, Rebecca; Rao, Kanchan; Henter, Jan-Inge; Jordan, Michael; Filipovich, Lisa; Bader, Peter; Beier, Rita; Burkhardt, Birgit; Meisel, Roland; Schulz, Ansgar; Winkler, Beate; Albert, Michael H.; Greil, Johann; Karasu, Gülsün; Woessmann, Wilhelm; Corbacioglu, Selim; Gruhn, Bernd; Holter, Wolfgang; Kühl, Jörn-Sven; Lang, Peter; Seidel, Markus G.; Veys, Paul; Löfstedt, Alexandra; Ammann, Sandra; Ehl, Stephan; Janka, Gritta; Müller, Ingo und Lehmberg, Kai
(2016):
The minimum required level of donor chimerism in hereditary hemophagocytic lymphohistiocytosis.
In: Blood, Bd. 127, Nr. 25: S. 3281-3290