Associated Papers
Identification of a mutation in TNRC18 in a patient with clinical features of Fazio-Londe disease.
Khani M et al.
Clinical Case Reports, 2024
38188848 (PubMed )
Supplement: CCR3-12-e8394-s001.xlsx › Sheet1
NCI-60 whole exome sequencing and pharmacological CellMiner analyses.
Reinhold WC et al.
Plos One, 2014
25032700 (PubMed )
Supplement: pone.0101670.s001.xlsx › Supplementary_Table_1
Select a paper to view details