Fig. 1From: A novel deletion variant in TRAPPC2 causes spondyloepiphyseal dysplasia tarda in a five-generation Chinese familyFamily pedigree of the Chinese family with short stature. Individuals include: males (squares), females (circles), deceased individuals (symbols with a crossing line), unaffected individuals (open symbol), affected individuals (slashed symbol), and X-linked carriers (denoted with a dot in the middle of symbol)Back to article page