Fig. 4From: A novel mutation in EYA1 in a Chinese family with Branchio-oto-renal syndromeEYA1 gene test in this family revealed a novel heterozygous nonsense variation (c.967A > T; p: Arg323X) in exon 11 in members with various physical anomalies (II:2, III:6, III:1, and III:2) (arrow). The normal family members harbored no mutations in EYA1Back to article page