Associated Papers
PIK3CA mutation in a case of CTNNB1-mutant sinonasal glomangiopericytoma.
Hong CS et al.
Cold Spring Harbor Molecular Case Studies, 2022
Adrenocortical Tumors in Children With Constitutive Chromosome 11p15 Paternal Uniparental Disomy: Implications for Diagnosis and Treatment.
Pinto EM et al.
Frontiers in Endocrinology, 2021
Detection of beta-catenin mutations in paraffin-embedded sporadic desmoid-type fibromatosis by mutation-specific restriction enzyme digestion (MSRED): an ancillary diagnostic tool.
Amary MF et al.
The American Journal of Surgical Pathology, 2007
Select a paper to view details