APA

Frykholm C., Klar J., Arnesson H., Rehnman A., Lodahl M., Wedén U., Dahl N., Tranebjærg L. & Rendtorff N. D. (20150625). Phenotypic variability in a seven-generation Swedish family segregating autosomal dominant hearing impairment due to a novel EYA4 frameshift mutation. : Gene.

Chicago

Frykholm Carina, Klar Joakim, Arnesson Hanna, Rehnman Anna-Carin, Lodahl Marianne, Wedén Ulla, Dahl Niklas, Tranebjærg Lisbeth and Rendtorff Nanna D. 20150625. Phenotypic variability in a seven-generation Swedish family segregating autosomal dominant hearing impairment due to a novel EYA4 frameshift mutation. : Gene.

Harvard

Frykholm C., Klar J., Arnesson H., Rehnman A., Lodahl M., Wedén U., Dahl N., Tranebjærg L. and Rendtorff N. D. (20150625). Phenotypic variability in a seven-generation Swedish family segregating autosomal dominant hearing impairment due to a novel EYA4 frameshift mutation. : Gene.

MLA

Frykholm Carina, Klar Joakim, Arnesson Hanna, Rehnman Anna-Carin, Lodahl Marianne, Wedén Ulla, Dahl Niklas, Tranebjærg Lisbeth and Rendtorff Nanna D. Phenotypic variability in a seven-generation Swedish family segregating autosomal dominant hearing impairment due to a novel EYA4 frameshift mutation. : Gene. 20150625.