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Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 Deletion Syndrome
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- Gur R; Warren S
- Creator
Metadata
- Published
- 2020-01-01
- DOI
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- 10.15154/1519190
- Publisher
- NIMH Data Repositories
- Creator Name (e-Rad)
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- Gur R; Warren S