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Fig. 1 | BMC Medical Genomics

Fig. 1

From: Whole-exome sequencing identified a novel heterozygous mutation of SALL1 and a new homozygous mutation of PTPRQ in a Chinese family with Townes-Brocks syndrome and hearing loss

Fig. 1

Clinical data for the family. a Pedigree of this family. Square indicates male, circle indicates female, and arrow indicates the proband. b Proband’s X-ray with anorectal deformity and fistula. c X-rays of the proband’s hands with a multifinger phenotype. d External ear deformity of the proband’s father. e Toe deformities of the proband’s father

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