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Dive into the research topics of 'De novo mutations in CSNK2A1 are associated with neurodevelopmental abnormalities and dysmorphic features'. Together they form a unique fingerprint.- Sort by
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Volkan Okur, Megan T. Cho, Lindsay Henderson, Kyle Retterer, Michael Schneider, Shannon Sattler, Dmitriy Niyazov, Meron Azage, Sharon Smith, Jonathan Picker, Sharyn Lincoln, Mark Tarnopolsky, Lauren Brady, Hans T. Bjornsson, Carolyn Applegate, Amy Dameron, Rebecca Willaert, Berivan Baskin, Jane Juusola, Wendy K. Chung
Research output: Contribution to journal › Article › peer-review