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. 2016 Nov 14;8(12):1455–1469. doi: 10.15252/emmm.201606623

Figure 1. Damaging variants in SHOX and CYP26C1 in patients with LWD .

Figure 1

  1. Pedigree of family 1. Individuals II:3 and III:2 were analyzed by whole‐exome sequencing. Damaging variants in SHOX and CYP26C1 co‐segregate with LWD.
  2. Pedigrees of families 2 and 3.
Data information: filled symbol, LWD‐affected individual; symbol with a slash, deceased individual; slash, divorced; red text, SHOX locus; green text, CYP26C1 locus; +, wild‐type allele; N.A., DNA not available; arrow, index patient.