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3. Early detection of adrenocortical carcinoma in a child with Li-Fraumeni syndrome. Lin MT, Shieh JJ, Chang JH, Chang SW, Chen TC, Hsu WH. Pediatr Blood Cancer; 2009 Apr; 52(4):541-4. PubMed ID: 19101993 [Abstract] [Full Text] [Related]
4. Li-Fraumeni and Li-Fraumeni-like syndrome among children diagnosed with pediatric cancer in Southern Brazil. Giacomazzi J, Selistre SG, Rossi C, Alemar B, Santos-Silva P, Pereira FS, Netto CB, Cossio SL, Roth DE, Brunetto AL, Zagonel-Oliveira M, Martel-Planche G, Goldim JR, Hainaut P, Camey SA, Ashton-Prolla P. Cancer; 2013 Dec 15; 119(24):4341-9. PubMed ID: 24122735 [Abstract] [Full Text] [Related]
5. Two Li-Fraumeni syndrome families with novel germline p53 mutations: loss of the wild-type p53 allele in only 50% of tumours. Sedlacek Z, Kodet R, Kriz V, Seemanova E, Vodvarka P, Wilgenbus P, Mares J, Poustka A, Goetz P. Br J Cancer; 1998 Apr 15; 77(7):1034-9. PubMed ID: 9569035 [Abstract] [Full Text] [Related]
7. TP53 and CDKN1A mutation analysis in families with Li-Fraumeni and Li-Fraumeni like syndromes. Andrade RC, Dos Santos AC, de Aguirre Neto JC, Nevado J, Lapunzina P, Vargas FR. Fam Cancer; 2017 Apr 15; 16(2):243-248. PubMed ID: 27714481 [Abstract] [Full Text] [Related]
8. Novel germline mutation of the p53 tumor suppressor gene in a child with incidentally discovered adrenal cortical carcinoma. Grayson GH, Moore S, Schneider BG, Saldivar V, Hensel CH. Am J Pediatr Hematol Oncol; 1994 Nov 15; 16(4):341-7. PubMed ID: 7978053 [Abstract] [Full Text] [Related]
9. [Germline mutations of the p53 gene]. Frebourg T. Pathol Biol (Paris); 1997 Dec 15; 45(10):845-51. PubMed ID: 9769948 [Abstract] [Full Text] [Related]
10. A new germline TP53 gene mutation in a family with Li-Fraumeni syndrome. Dockhorn-Dworniczak B, Wolff J, Poremba C, Schäfer KL, Ritter J, Gullotta F, Jürgens H, Böcker W. Eur J Cancer; 1996 Jul 15; 32A(8):1359-65. PubMed ID: 8869100 [Abstract] [Full Text] [Related]
11. Novel p53 germline mutation in a patient with Li-Fraumeni syndrome. Wong SS, Lozano G, Gaff CL, Gardner RJ, Strong LC, Aittomäki K, Lindeman GJ. Intern Med J; 2003 Dec 15; 33(12):621. PubMed ID: 14656244 [No Abstract] [Full Text] [Related]
12. Tumor-specific mutations in p53: the acid test. Hainaut P. Nat Med; 2002 Jan 15; 8(1):21-3. PubMed ID: 11786899 [No Abstract] [Full Text] [Related]
13. [A method for detection of germinal mutations in the p53 tumor suppressor gene]. Sedlácek Z, Kríz V, Seemanová E, Vlcek C, Maríková T, Mares J, Goetz P. Cas Lek Cesk; 1996 Dec 04; 135(23):762-7. PubMed ID: 9005123 [Abstract] [Full Text] [Related]
14. A Li-Fraumeni syndrome family with retained heterozygosity for a germline TP53 mutation in two tumors. Trkova M, Foretova L, Kodet R, Hedvicakova P, Sedlacek Z. Cancer Genet Cytogenet; 2003 Aug 04; 145(1):60-4. PubMed ID: 12885464 [Abstract] [Full Text] [Related]
15. The first documentation of Li-Fraumeni syndrome in Korea. Bang YJ, Kang SH, Kim TY, Jung CW, Oh SM, Choe KJ, Kim NK. J Korean Med Sci; 1995 Jun 04; 10(3):205-10. PubMed ID: 8527048 [Abstract] [Full Text] [Related]
16. p53 Tetramerization domain mutations: germline R342X and R342P, and somatic R337G identified in pediatric patients with Li-Fraumeni syndrome and a child with adrenocortical carcinoma. Fiszer-Maliszewska L, Kazanowska B, Padzik J, Regional Blood Transfusion Center. Fam Cancer; 2009 Jun 04; 8(4):541-6. PubMed ID: 19714490 [Abstract] [Full Text] [Related]
17. Three germline mutations in the TP53 gene. Cornelis RS, van Vliet M, van de Vijver MJ, Vasen HF, Voute PA, Top B, Khan PM, Devilee P, Cornelisse CJ. Hum Mutat; 1997 Jun 04; 9(2):157-63. PubMed ID: 9067756 [Abstract] [Full Text] [Related]
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19. [Li Fraumeni syndrome: a case with multiple primary cancers and presenting a germline p53 mutation]. Landolsi S, Gharbi O, Zrig M, Gribaa M, Njim L, Zakhama A, Abid A, Frébourg T, Ahmed SB. Ann Biol Clin (Paris); 2010 Nov 04; 68(3):346-50. PubMed ID: 20478780 [Abstract] [Full Text] [Related]
20. p53 germline mutations in Li-Fraumeni syndrome. Santibáñez-Koref MF, Birch JM, Hartley AL, Jones PH, Craft AW, Eden T, Crowther D, Kelsey AM, Harris M. Lancet; 1991 Dec 14; 338(8781):1490-1. PubMed ID: 1683921 [Abstract] [Full Text] [Related] Page: [Next] [New Search]