Bainbridge-Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition

Kuechler, Alma; Czeschik, Johanna Christina; Graf, Elisabeth; Grasshoff, Ute; Hueffmeier, Ulrike; Busa, Tiffany; Beck-Woedl, Stefanie; Faivre, Laurence; Riviere, Jean-Baptiste; Bader, Ingrid; Koch, Johannes; Reis, Andre; Hehr, Ute; Rittinger, Olaf; Sperl, Wolfgang; Haack, Tobias B.; Wieland, Thomas; Engels, Hartmut; Prokisch, Holger; Strom, Tim M.; Luedecke, Hermann-Josef; Wieczorek, Dagmar

Bainbridge-Ropers syndrome caused by loss-of-function variants in ASXL3: a recognizable condition

Autor(en):

Kuechler, Alma; Czeschik, Johanna Christina; Graf, Elisabeth; Grasshoff, Ute; Hueffmeier, Ulrike; Busa, Tiffany; Beck-Woedl, Stefanie; Faivre, Laurence; Riviere, Jean-Baptiste; Bader, Ingrid; Koch, Johannes; Reis, Andre; Hehr, Ute; Rittinger, Olaf; Sperl, Wolfgang; Haack, Tobias B.; Wieland, Thomas; Engels, Hartmut; Prokisch, Holger; Strom, Tim M.; Luedecke, Hermann-Josef; Wieczorek, Dagmar

Tübinger Autor(en):

Grasshoff, Ute
Beck-Wödl, Stefanie

Erschienen in:

European Journal of Human Genetics (2017), Bd. 25, H. 2, S. 183-191

Verlagsangabe:

Nature Publishing Group

Sprache:

Englisch

Referenz zum Volltext:

http://dx.doi.org/10.1038/ejhg.2016.165

ISSN:

1476-5438