Additional file 3: Table S3. of Clinical diagnostic exome evaluation for an infant with a lethal disorder: genetic diagnosis of TARP syndrome and expansion of the phenotype in a patient with a newly reported RBM10 alteration PowisZรถe HartAlexa ChernySara PetrikIgor PalmaerErika TangSha JonesCarolyn 2017 List of candidate genes/alterations resulting from inheritance model filtering and the manual removal of NGS artifacts and polymorphisms*. (DOCX 18 kb)