English
Somatic mutation spectrum of a Chinese cohort of pediatrics with vascular malformations
Source: Orphanet Journal of Rare Diseases
Targeted next-generation sequencing for detection of PIK3CA mutations in archival tissues from patients with Klippel–Trenaunay syndrome in an Asian population: List the full names and institutional addresses for all authors
Source: Orphanet Journal of Rare Diseases
Klippel–Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review
Source: Children
Bilateral Wilms Tumor in CLOVES Syndrome
Source: Urology
The emerging role of PI3K inhibitors for solid tumour treatment and beyond
Source: British Journal of Cancer