The Survey of Syndromes with the Risk of Cancer in Children Age
Authors:
V. Krutílková 1; T. Eckschlager 2
Authors‘ workplace:
Gennet, s. r. o., Praha 2Klinika dětské hematologie a onkologie, 2. LF UK a FN Motol, Praha
1
Published in:
Klin Onkol 2009; 22(Supplementum): 45-49
Sources
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5. Frohnmayer L, Frohnmayer D. Fanconi Anemia: A handbook for families and their physicians. 3rd ed. Eugene: Fanconi Anemia Research Fund, Inc. 2000.
6. Lindor NM, Greene MH and the Mayo Familial Cancer Program. The concise handbook of family cancer syndromes. J Natl Cancer Inst 1998; 90: 1039–1071.
7. Pizzo PA, Poplack DG. Principles and practice of pediatric oncology. Philadelphia: Lippincot, Wiliams & Wilkins 2006.
8. Plevová P, Šilhánová E, Foretová L. Vzácné hereditární syndromy s vyšším rizikem vzniku nádorů. Klin Onkol 2006; 19(Suppl): 68–75.
9. Scott RH, Stiller CA, Walker L et al. Syndromes and constitutional chromosomal abnormalities associated with Wilms tumour. J Med Genet 2006; 43: 705–715.
10. Seemannová E, Karolín P. Nijmegen breakage syndrome (NBS). Čs Pediatrie 1999; 54(2): 97–1001.
Labels
Paediatric clinical oncology Surgery Clinical oncologyArticle was published in
Clinical Oncology
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