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Fig. 4 | BMC Medical Genetics

Fig. 4

From: A heterozygous duplication variant of the HOXD13 gene caused synpolydactyly type 1 with variable expressivity in a Chinese family

Fig. 4

Sequence analysis of HOXD13 mutation in the Chinese family. a, Sanger sequencing result of the unaffected member (V-2) done after PCR showing no double peaks. b, Sanger sequencing result of the diseased (V-1) done after PCR showing double peaks at duplication site. c, Sanger sequencing result of the affected member (IV-11) done after PCR showing double peaks at duplication site

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