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. Author manuscript; available in PMC: 2017 Jul 5.
Published in final edited form as: N Engl J Med. 2016 Dec 7;376(1):21–31. doi: 10.1056/NEJMoa1516767

Figure 3. Blended Phenotypes among Patients with Dual Diagnoses.

Figure 3

Dual molecular diagnoses may result from variants at two loci (Gene A and Gene B) and can result in distinct clinical features (Panel A) or similar phenotypic features (Panel B).

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