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From Statistical Genetics Courses
'''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. (submittdsubmitted)
* 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)
* Hirsch S, Elling C, Bootpetch Roberts TC, Scholes MA, Hafrén L. Streubel SO, Pine HS, Wine TM, Szeremeta W, Prager JD, Elisabet Einarsdottir E, Yousaf A, Baschal EE, Sakina Rehman S, University of Washington Center for Mendelian Genomics, Bamshad MJ, Nickerson DA, Riazuddin S, Leal SM, Ahmed ZM, Yoon PJ, Kere J, Chan KH, MattilaPS, Norman R. Friedman NR, Chonmaitree T, Frank DN, Ryan AF, Santos-Cortez RLP (2020) The role of ''CDHR3 ''in susceptibility to otitis media (submitted)
