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. Author manuscript; available in PMC: 2016 Sep 1.
Published in final edited form as: Am J Med Genet A. 2015 Apr 29;0(9):2114–2121. doi: 10.1002/ajmg.a.37138

Figure 1.

Figure 1

Patient pedigrees and mutations. Probands are indicated as filled circles (all are females). For HC4, the father was unavailable and is denoted in gray. Implicated causal mutations are shown underneath each trio.