Associated Papers
Genetic and epigenetic features of bilateral Wilms tumor predisposition in patients from the Children's Oncology Group AREN18B5-Q.
Murphy AJ et al.
Nature Communications, 2023
38110397 (PubMed )
Supplement: 41467_2023_43730_MOESM5_ESM.xlsx › COG
Cyclin-dependent kinases and rare developmental disorders.
Colas P
Orphanet Journal of Rare Diseases, 2020
De Novo Missense Substitutions in the Gene Encoding CDK8, a Regulator of the Mediator Complex, Cause a Syndromic Developmental Disorder.
Calpena E et al.
American Journal of Human Genetics, 2019
30905399 (PubMed )
Supplement: mmc4.pdf
Select a paper to view details