Figure 1: Pedigree of the six Roifman Syndrome cases (kindred 1–4).

The pedigrees show the RNU4ATAC compound heterozygous SNVs in the six genotyped cases of Roifman Syndrome; [=] indicates no variant detected.
The pedigrees show the RNU4ATAC compound heterozygous SNVs in the six genotyped cases of Roifman Syndrome; [=] indicates no variant detected.