James Lawlor
HudsonAlpha Institute for Biotechnology
33 papers found
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P3-143: Utility of Genomic Sequencing in Cases of Early-Onset and Familial Dementia
UploadDeleterious Variation in BRSK2 Associates with a Neurodevelopmental Disorder
UploadSystematic reanalysis of genomic data improves quality of variant interpretation
UploadGenomic sequencing identifies secondary findings in a cohort of parent study participants
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