Associated Papers
High-frequency actionable pathogenic exome variants in an average-risk cohort.
Rego S et al.
Cold Spring Harbor Molecular Case Studies, 2018
30487145 (PubMed )
Supplement: supp_mcs.a003178_Supplemental_File_3.xlsx › Sheet1
CCDC22: a novel candidate gene for syndromic X-linked intellectual disability.
Voineagu I et al.
Molecular Psychiatry, 2012
Select a paper to view details