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Fig. 1 | BMC Medical Genomics

Fig. 1

From: Identification of a novel heterozygous missense TP63 variant in a Chinese pedigree with split-hand/foot malformation

Fig. 1

Family pedigree, clinical phenotype, and Sanger sequencing results of individuals who were subjected to WES. a A consanguineous pedigree showing four affected members (II-4, II-5, III-2, and IV-1) in the four-generation family. b Clinical features of the affected individuals, II-4, II-5, III-2, and IV-1. c The Sanger sequencing results of II-4, II-5, III-1, III-2, and IV-1. The red arrows indicated the substitution

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BMC Medical Genomics

ISSN: 1755-8794

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