Andreas Kirchnawy

Whole-exome sequencing to identify the cause of congenital sensorineural hearing loss in carriers of a heterozygous GJB2 mutation

B. Streubel, T. Parzefall, K. Frei, 2017, European Archives of Oto-Rhino-Laryngology.

Identification of a rare COCH mutation by whole-exome sequencing

W. Gstoettner, B. Streubel, T. Parzefall, 2017, Wiener klinische Wochenschrift.

Identification of a rare COCH mutation by whole-exome sequencing

W. Gstoettner, B. Streubel, T. Parzefall, 2017, Wiener klinische Wochenschrift.