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. Author manuscript; available in PMC: 2019 Mar 14.
Published in final edited form as: J Med Genet. 2014 Apr 17;51(6):413–418. doi: 10.1136/jmedgenet-2013-102249

Figure 1.

Figure 1

(A) Infant image of a patient with frameshift mutation in GLI2. (B) Same patient as (A) in early childhood. (C) Infant image of a patient with nonsense mutation in GLI2. (D) Same patient as (C) in early childhood. (E/F) Frontal and side views of infant with frameshift mutation in GLI2. (G) Infant with deletion of GLI2. (H) Mother of G (as an infant), with same deletion.