Vos JR

ORCID: 0000-0001-8802-7002 · 1 paper in corpus · active 2025
2025
Clinical genetics ·doi:10.1111/cge.14759

PTEN Hamartoma Tumor Syndrome (PHTS) is a rare hereditary syndrome. PHTS has a variable phenotype characterized by benign lesions and increased cancer risks. Clarifying the extent of the benign phenotype could facilitate early recognition o…