Co-Authors
This is a "connection" page, showing publications co-authored by LINDSAY BURRAGE and MERED PARNES.
Connection Strength
0.221
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Novel deletion of 6p21.31p21.1 associated with laryngeal cleft, developmental delay, dysmorphic features and vascular anomaly. Eur J Med Genet. 2019 Jun; 62(6):103531.
Score: 0.161
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Gain-of-function and loss-of-function variants in GRIA3 lead to distinct neurodevelopmental phenotypes. Brain. 2024 May 03; 147(5):1837-1855.
Score: 0.060