APA
Spiegler S., Najm J., Liu J., Gkalympoudis S., Schröder W., Borck G., Brockmann K., Elbracht M., Fauth C., Ferbert A., Freudenberg L., Grasshoff U., Hellenbroich Y., Henn W., Hoffjan S., Hüning I., Korenke G. C., Kroisel P. M., Kunstmann E., Mair M., Munk-Schulenburg S., Nikoubashman O., Pauli S., Rudnik-Schöneborn S., Sudholt I., Sure U., Tinschert S., Wiednig M., Zoll B., Ginsberg M. H. & Felbor U. (20140401). High mutation detection rates in cerebral cavernous malformation upon stringent inclusion criteria: one-third of probands are minors. : Molecular genetics & genomic medicine.
Chicago
Spiegler Stefanie, Najm Juliane, Liu Jian, Gkalympoudis Stephanie, Schröder Winnie, Borck Guntram, Brockmann Knut, Elbracht Miriam, Fauth Christine, Ferbert Andreas, Freudenberg Leonie, Grasshoff Ute, Hellenbroich Yorck, Henn Wolfram, Hoffjan Sabine, Hüning Irina, Korenke G Christoph, Kroisel Peter M, Kunstmann Erdmute, Mair Martina, Munk-Schulenburg Susanne, Nikoubashman Omid, Pauli Silke, Rudnik-Schöneborn Sabine, Sudholt Irene, Sure Ulrich, Tinschert Sigrid, Wiednig Michaela, Zoll Barbara, Ginsberg Mark H and Felbor Ute. 20140401. High mutation detection rates in cerebral cavernous malformation upon stringent inclusion criteria: one-third of probands are minors. : Molecular genetics & genomic medicine.
Harvard
Spiegler S., Najm J., Liu J., Gkalympoudis S., Schröder W., Borck G., Brockmann K., Elbracht M., Fauth C., Ferbert A., Freudenberg L., Grasshoff U., Hellenbroich Y., Henn W., Hoffjan S., Hüning I., Korenke G. C., Kroisel P. M., Kunstmann E., Mair M., Munk-Schulenburg S., Nikoubashman O., Pauli S., Rudnik-Schöneborn S., Sudholt I., Sure U., Tinschert S., Wiednig M., Zoll B., Ginsberg M. H. and Felbor U. (20140401). High mutation detection rates in cerebral cavernous malformation upon stringent inclusion criteria: one-third of probands are minors. : Molecular genetics & genomic medicine.
MLA
Spiegler Stefanie, Najm Juliane, Liu Jian, Gkalympoudis Stephanie, Schröder Winnie, Borck Guntram, Brockmann Knut, Elbracht Miriam, Fauth Christine, Ferbert Andreas, Freudenberg Leonie, Grasshoff Ute, Hellenbroich Yorck, Henn Wolfram, Hoffjan Sabine, Hüning Irina, Korenke G Christoph, Kroisel Peter M, Kunstmann Erdmute, Mair Martina, Munk-Schulenburg Susanne, Nikoubashman Omid, Pauli Silke, Rudnik-Schöneborn Sabine, Sudholt Irene, Sure Ulrich, Tinschert Sigrid, Wiednig Michaela, Zoll Barbara, Ginsberg Mark H and Felbor Ute. High mutation detection rates in cerebral cavernous malformation upon stringent inclusion criteria: one-third of probands are minors. : Molecular genetics & genomic medicine. 20140401.