Hereditary Pediatric and Rare Cancers Resources
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Germline Mutations in Predisposition Genes in Pediatric Cancer
Zhang et al
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Second Surgery and the Prognosis of Choroid Plexus Carcinoma – Results of a Meta-analysis of Individual Cases
Wrede et al
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Whole-body magnetic resonance imaging (WB-MRI) as surveillance for subsequent malignancies in survivors of hereditary retinoblastoma: A pilot study
Friedman et al
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Whole body magnetic resonance imaging (WB-MRI) and brain MRI baseline surveillance in TP53 germline mutation carriers: experience from the Li-Fraumeni Syndrome Education and Early Detection (LEAD) clinic
Bojadzieva et al
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Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: 11 year follow-up of a prospective observational study
Villani et al
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Sarcomas Associated With Genetic Cancer Predisposition Syndromes: A Review
Farid et al
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Genotype–phenotype associations among panel-based TP53+ subjects
Rana et al
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A Rare TP53 Mutation Predominant in Ashkenazi Jews Confers Risk of Multiple Cancers
Powers et al
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Easing the Burden: Describing the Role of Social, Emotional and Spiritual Support in Research Families with Li-Fraumeni Syndrome
Peters et al
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