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Journal Abstract Search

207 related items for PubMed ID: 18786442

  • 1. Li-Fraumeni syndrome in a Malaysian kindred.
    Ariffin H, Martel-Planche G, Daud SS, Ibrahim K, Hainaut P.
    Cancer Genet Cytogenet; 2008 Oct; 186(1):49-53. PubMed ID: 18786442
    [Abstract] [Full Text] [Related]

  • 2. 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
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  • 3. The first case of Li-Fraumeni syndrome in Bosnia and Herzegovina: case report.
    Vranic S, Kapur L, Foco F, Bilalovic N, Hainaut P.
    Pathologica; 2006 Apr; 98(2):156-9. PubMed ID: 16929790
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  • 6. Recognition of Li Fraumeni syndrome at diagnosis of a locally advanced extremity rhabdomyosarcoma.
    Trahair T, Andrews L, Cohn RJ.
    Pediatr Blood Cancer; 2007 Mar; 48(3):345-8. PubMed ID: 16534790
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  • 7. Germ-line splicing mutation of the p53 gene in a cancer-prone family.
    Warneford SG, Witton LJ, Townsend ML, Rowe PB, Reddel RR, Dalla-Pozza L, Symonds G.
    Cell Growth Differ; 1992 Nov; 3(11):839-46. PubMed ID: 1467311
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  • 8. Balanced t(11;15)(q23;q15) in a TP53+/+ breast cancer patient from a Li-Fraumeni syndrome family.
    Sherif ZA, Danielsen M.
    Cancer Genet Cytogenet; 2006 Jul 01; 168(1):50-8. PubMed ID: 16772121
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  • 10. Complex replication error causes p53 mutation in a Li-Fraumeni family.
    Strauss EA, Hosler MR, Herzog P, Salhany K, Louie R, Felix CA.
    Cancer Res; 1995 Aug 01; 55(15):3237-41. PubMed ID: 7614454
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  • 12. Identification of a novel p53 in-frame deletion in a Li-Fraumeni-like family.
    Schiffman JD, Chun N, Fisher PG, Dahl GV, Ford JM, Eggerding FA.
    Pediatr Blood Cancer; 2008 Apr 01; 50(4):914-6. PubMed ID: 17554785
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  • 13. [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 Apr 01; 68(3):346-50. PubMed ID: 20478780
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  • 14. Clinical spectrum of Li-Fraumeni syndrome/Li-Fraumeni-like syndrome in Brazilian individuals with the TP53 p.R337H mutation.
    Ferreira AM, Brondani VB, Helena VP, Charchar HLS, Zerbini MCN, Leite LAS, Hoff AO, Latronico AC, Mendonca BB, Diz MDPE, de Almeida MQ, Fragoso MCBV.
    J Steroid Biochem Mol Biol; 2019 Jun 01; 190():250-255. PubMed ID: 30974190
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  • 15. 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 01; 16(4):341-7. PubMed ID: 7978053
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  • 17. Familial aggregation of soft tissue sarcomas: a report of three cases from a Li-Fraumeni-like family.
    Narita T, Dobashi Y, Nakamura T, Yokoyama S, Matsuda K.
    Arch Pathol Lab Med; 1997 May 01; 121(5):493-8. PubMed ID: 9167603
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  • 19. p53 mosaicism with an exon 8 germline mutation in the founder of a cancer-prone pedigree.
    Kovar H, Auinger A, Jug G, Müller T, Pillwein K.
    Oncogene; 1992 Nov 01; 7(11):2169-73. PubMed ID: 1359493
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  • 20. Overexpression of the retinoblastoma gene in a familial adrenocortical carcinoma.
    Warneford S, Townsend M, Rowe PB, Dalla-Pozza L, Symonds G.
    Cell Growth Differ; 1991 Sep 01; 2(9):439-45. PubMed ID: 1751410
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