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Fig. 1 | BMC Medical Genomics

Fig. 1

From: Novel mutation in the TGFBI gene in a Moroccan family with atypical corneal dystrophy: a case report

Fig. 1

Pedigree of a four-generation family affected by Thiel-Behnke corneal dystrophy. The pedigree shows an autosomal dominant transmission of the disease. The arrow indicates the proband, the filled symbols indicate affected subjects, and open symbols represent unaffected individuals. Squares represent males, and circles represent females. A slash mark through the square or circle indicates deceased individuals

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