Show 5 5 10 15 20 50 100 250 Sort by year (new to old) Actions Download search results Subscribe to news feed Your filters: cql: author="Tabatabaiefar, Mohammad Amin" or (type any "bookEditor journalEditor issueEditor" and edi... Add to list Journal Article A1 open access Molecular diagnostics for congenital hearing loss including 15 deafness genes using a next generation sequencing platform Sarah De Keulenaer (UGent) , Jan Hellemans, Steve Lefever (UGent) , Jean-Pierre Renard (UGent) , Joachim De Schrijver (UGent) , Hendrik Van de Voorde (UGent) , Mohammad Amin Tabatabaiefar, Filip Van Nieuwerburgh (UGent) , Daisy Flamez (UGent) , Filip Pattyn (UGent) , et al. (2012) BMC MEDICAL GENOMICS. 5. Add to list Journal Article A1 A mutation in CABP2, expressed in cochlear hair cells, causes autosomal-recessive hearing impairment Isabelle Schrauwen, Sarah Helfmann, Akira Inagaki, Friederike Predoehl, Mohammad Amin Tabatabaiefar, Maria Magdalena Picher, Manou Sommen, Celia Zazo Seco, Jaap Oostrik, Hannie Kremer, et al. (2012) AMERICAN JOURNAL OF HUMAN GENETICS. 91(4). p.636-645