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
1. OMIM – Online Mendelian Inheritance in Man. Dostupné z http://www.ncbi.nlm.nih.gov/sites/entrez?db=omim&TabCmd=Limits.
2. Dokal I. Fanconi anemia is a highly penetrant cancer susceptibility cancer syndrome. Hematologica 2008; 93(4): 486–488.
3. Eeles RA, Easton DF, Poder BAJ et al (eds). Genetic Predisposition to Cancer. 2nd ed. Oxford: Hodder Arnold 2004.
4. Federman N, Sakamoto KM. Topics in pediatrics leukemia – Fanconi’s anemia. Med Gen Med 2005; 7(2): 23.
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.
11. www.emedicine.com
12. www.genetests.org
Don‘t have an account? Create new account
Enter the email address that you registered with. We will send you instructions on how to set a new password.
