Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: 11 year follow-up of a prospective observational study

Author:

Villani Anita,Shore Ari,Wasserman Jonathan D,Stephens Derek,Kim Raymond H,Druker Harriet,Gallinger Bailey,Naumer Anne,Kohlmann Wendy,Novokmet Ana,Tabori Uri,Tijerin Marta,Greer Mary-Louise C,Finlay Jonathan L,Schiffman Joshua D,Malkin David

Publisher

Elsevier BV

Subject

Oncology

Reference21 articles.

1. Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study;Villani;Lancet Oncol,2011

2. The benefit and burden of cancer screening in Li-Fraumeni syndrome: a case report;Jhaveri;Yale J Biol Med,2015

3. Germ-line p53 mutations predispose to a wide spectrum of early-onset cancers;Nichols;Cancer Epidemiol Biomarkers Prev,2001

4. ARCAD: a method for estimating age-dependent disease risk associated with mutation carrier status from family data;Le Bihan;Genet Epidemiol,1995

5. Role of rapid sequence whole-body MRI screening in SDH-associated hereditary paraganglioma families;Jasperson;Fam Cancer,2014

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