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Figure 1 | BMC Medical Genetics

Figure 1

From: Intergenerational and intrafamilial phenotypic variability in 22q11.2 Deletion syndrome subjects

Figure 1

Intrafamilial phenotypic comparison. A higher number of features were observed in the second generation in 23 couples. In 6 couples the number of features was higher in the parents’ generation and in the remaining 3 couples no difference was found. The brackets indicate the families with 2 or more second generation affected subjects. * indicates the proband within these families.

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