Using common genetic variation to examine phenotypic expression and risk prediction in 22q11.2 deletion syndrome
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Origin | Files produced by the author(s) |
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Léa Mosnier : Connect in order to contact the contributor
https://amu.hal.science/hal-03222249
Submitted on : Thursday, September 28, 2023-12:05:19 PM
Last modification on : Wednesday, May 22, 2024-9:16:11 AM