Fig. 2From: Prenatal diagnosis identifies compound heterozygous variants in RYR1 that causes ultrasound abnormalities in a fetusSanger sequencing validation of RYR1 variants identified by exome sequencing. A Variant c. 2682G > C in the RYR1 gene in heterozygous state (father). B Variant c. 12572G > A in the RYR1 gene in heterozygous state (mother)Back to article page