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Sanger sequencing of the proband in the region about the mutations in the FGFR3 gene. There were two heterozygous mutations of the c.1133G>A and the c.1138G>A (a). The allele‐specific PCR revealed that the c.1133G>A and the c.1138G>A were in the same allele (b), while no mutations were detected in another allele (c)
