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Fig. 2 | BMC Medical Genetics

Fig. 2

From: Dual molecular diagnosis of tricho-rhino-phalangeal syndrome type I and Okur-Chung neurodevelopmental syndrome in one Chinese patient: a case report

Fig. 2

a Patient’s family’s pedigree. Black arrow shows the proband. Black square indicates the patient affected with OCNDS caused by a variant in the CSNK2A1 gene. Square filled with transverse lines indicates the patient affected with TRPS I caused by a variant in the TRPS1 gene. The compound heterozygote found in this patient was vertically transmitted from his father and mother respectively; b Validation by Sanger sequencing of CSNK2A1 and TRPS1 gene in this family

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