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Clinical and genetic features of 3 patients with familial chylomicronemia due to mutations in GPIHBP1 gene
Wyllie R, Hyams JS, Kay M
For example, clear cell sarcoma (CCS) clinically presents as a deep and small ( 3.0.CO;2-A
HR is deficient in many tumours, leading to increased sensitivity to DNA-damaging agents that are used widely in clinical settings
