Publications
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Author Title [ Year
] Filters: Keyword is Exome and Author is Scott, Daryl A [Clear All Filters]
Congenital heart defects and left ventricular non-compaction in males with loss-of-function variants in NONO. J Med Genet 54, 47-53 (2017).
De novo missense variants in PPP1CB are associated with intellectual disability and congenital heart disease. Hum Genet 135, 1399-1409 (2016).
