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Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: De novo deletions and duplications of 17q25.3 cause susceptibility to cardiovascular malformations

Fig. 1

Breakpoint mapping in eight subjects with 17q25 deletions and duplications (based on hg18). The red bars indicate deletion and green bars represent duplications. The first three photos (a, b, c) represent subjects with deletion. Individuals with duplication are shown in panels, d, e and f. Note the variability of phenotype related to genomic rearrangements in the group. Notably, when parents were tested, all events were apparently de novo (DN) in origin

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