Associated Papers
Challenges and opportunities in the investigation of unexplained intellectual disability using family-based whole-exome sequencing.
Helsmoortel C et al.
Clinical Genetics, 2015
Novel mutations target distinct subgroups of medulloblastoma.
Robinson G et al.
Nature, 2012
22722829 (PubMed )
Supplement: NIHMS374717-supplement-table_9.xlsx › Tier1
Select a paper to view details