Supplementary Figure 2: Probands with de novo CHD4 mutations. | Nature Genetics

Supplementary Figure 2: Probands with de novo CHD4 mutations.

From: Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing

Supplementary Figure 2

A) Clinical synopsis of the observed phenotypes across patients carrying CHD4 mutations. Columns represent single probands, shades of cells represent the number of probands sharing a phenotype in the given phenotypic categories. Photographs of affected probands are shown for which consent could be obtained for publication. B) Protein plot showing CHD4 protein domains and the distribution of de novo mutations.

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