APA
Geoffroy V., Stoetzel C., Scheidecker S., Schaefer E., Perrault I., Bär S., Kröll A., Delbarre M., Antin M., Leuvrey A., Henry C., Blanché H., Decker E., Kloth K., Klaus G., Mache C., Martin-Coignard D., McGinn S., Boland A., Deleuze J., Friant S., Saunier S., Rozet J., Bergmann C., Dollfus H. & Muller J. (20190614). Whole-genome sequencing in patients with ciliopathies uncovers a novel recurrent tandem duplication in IFT140. : Human mutation.
Chicago
Geoffroy Véronique, Stoetzel Corinne, Scheidecker Sophie, Schaefer Elise, Perrault Isabelle, Bär Séverine, Kröll Ariane, Delbarre Marion, Antin Manuela, Leuvrey Anne-Sophie, Henry Charline, Blanché Hélène, Decker Eva, Kloth Katja, Klaus Günter, Mache Christoph, Martin-Coignard Dominique, McGinn Steven, Boland Anne, Deleuze Jean-François, Friant Sylvie, Saunier Sophie, Rozet Jean-Michel, Bergmann Carsten, Dollfus Hélène and Muller Jean. 20190614. Whole-genome sequencing in patients with ciliopathies uncovers a novel recurrent tandem duplication in IFT140. : Human mutation.
Harvard
Geoffroy V., Stoetzel C., Scheidecker S., Schaefer E., Perrault I., Bär S., Kröll A., Delbarre M., Antin M., Leuvrey A., Henry C., Blanché H., Decker E., Kloth K., Klaus G., Mache C., Martin-Coignard D., McGinn S., Boland A., Deleuze J., Friant S., Saunier S., Rozet J., Bergmann C., Dollfus H. and Muller J. (20190614). Whole-genome sequencing in patients with ciliopathies uncovers a novel recurrent tandem duplication in IFT140. : Human mutation.
MLA
Geoffroy Véronique, Stoetzel Corinne, Scheidecker Sophie, Schaefer Elise, Perrault Isabelle, Bär Séverine, Kröll Ariane, Delbarre Marion, Antin Manuela, Leuvrey Anne-Sophie, Henry Charline, Blanché Hélène, Decker Eva, Kloth Katja, Klaus Günter, Mache Christoph, Martin-Coignard Dominique, McGinn Steven, Boland Anne, Deleuze Jean-François, Friant Sylvie, Saunier Sophie, Rozet Jean-Michel, Bergmann Carsten, Dollfus Hélène and Muller Jean. Whole-genome sequencing in patients with ciliopathies uncovers a novel recurrent tandem duplication in IFT140. : Human mutation. 20190614.