Fig. 2From: Abnormal eruption of teeth in relation to FGFR1 heterozygote mutation: a rare case of osteoglophonic dysplasia with 4-year follow-upThe exon gene sequencing results of the patient and his  parents, demonstrating FGFR1 (NM 023110.2) heterozygous mutation c.1121A>G in exon 9 in the patient (A), while his mother (B) and father (C) are normalBack to article page