'''Lasted updated: May, 2020'''
* Hussain S, Nawaz S, Khan H, Acharya A, Schrauwen I, Ahmad W, Leal SM (2020) A splice site variant in ''TCTN3'' underlies orofaciodigital syndrome IV. (submittd)
* Schrauwen I, Liaqat K, Bharadwaj T, Nasir A, Acharya A, Ahmad W, Leal SM (2020) An Autosomal Dominantly inherited variant in ''GREB1L'' causes profound sensorineural hearing impairment (submitted)