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De novo germline TP53 mutation presenting with synchronous malignancies of the central nervous system
Pediatric Blood & Cancer, 09/10/09
Schniederjan MJ et al. – This case identifies a rare, de novo, germline TP53 mutation presenting with synchronous CNS malignancies and exhibiting a more fulminant course than typical cases of Li–Fraumeni syndrome.
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Application with repeated serum biomarkers in pediatric appendicitis in clinical surgery
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High-risk neuroblastoma: a therapy in evolution
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