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
Klippel–Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review
Bilateral Wilms Tumor in CLOVES Syndrome
The emerging role of PI3K inhibitors for solid tumour treatment and beyond
Source: British Journal of Cancer
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