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. Author manuscript; available in PMC: 2018 Jun 1.
Published in final edited form as: Hum Genet. 2017 Mar 16;136(6):679–691. doi: 10.1007/s00439-017-1774-y

Fig. 1. Study flowchart.

Fig. 1

Two groups of patients (UW1 and Yale) were sequenced as part of a previous study (Longoni et al. 2014). The corresponding parental samples and additional complete trios were sequenced in batch UW2. A cohort of 39 full trios (DHREAMS, Yu et al. 2015) was also used for the de novo mutation analysis and enrichment calculations.