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Journal Abstract Search

168 related items for PubMed ID: 1557756

  • 21. Inherited p53 gene mutations in breast cancer.
    Sidransky D, Tokino T, Helzlsouer K, Zehnbauer B, Rausch G, Shelton B, Prestigiacomo L, Vogelstein B, Davidson N.
    Cancer Res; 1992 May 15; 52(10):2984-6. PubMed ID: 1581912
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  • 22. Li-Fraumeni syndrome in pediatric patients with soft tissue sarcoma or osteosarcoma.
    Carnevale A, Lieberman E, Cárdenas R.
    Arch Med Res; 1997 May 15; 28(3):383-6. PubMed ID: 9291635
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  • 23. Joint effects of germ-line p53 mutation and sex on cancer risk in Li-Fraumeni syndrome.
    Wu CC, Shete S, Amos CI, Strong LC.
    Cancer Res; 2006 Aug 15; 66(16):8287-92. PubMed ID: 16912210
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  • 24. Relative frequency and morphology of cancers in carriers of germline TP53 mutations.
    Birch JM, Alston RD, McNally RJ, Evans DG, Kelsey AM, Harris M, Eden OB, Varley JM.
    Oncogene; 2001 Aug 02; 20(34):4621-8. PubMed ID: 11498785
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  • 25. Is there anticipation in the age at onset of cancer in families with Li-Fraumeni syndrome?
    Trkova M, Hladikova M, Kasal P, Goetz P, Sedlacek Z.
    J Hum Genet; 2002 Aug 02; 47(8):381-6. PubMed ID: 12181637
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  • 26. [Cancer family syndrome in lung cancer--Li-Fraumeni syndrome in lung cancer].
    Tomita M, Tagawa Y, Tsuji T, Tsuji H, Ayabe H.
    Nihon Rinsho; 1995 Nov 02; 53(11):2716-21. PubMed ID: 8538032
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  • 27. Li-Fraumeni syndrome in a Malaysian kindred.
    Ariffin H, Martel-Planche G, Daud SS, Ibrahim K, Hainaut P.
    Cancer Genet Cytogenet; 2008 Oct 02; 186(1):49-53. PubMed ID: 18786442
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  • 28. The TP53 mutation, R337H, is associated with Li-Fraumeni and Li-Fraumeni-like syndromes in Brazilian families.
    Achatz MI, Olivier M, Le Calvez F, Martel-Planche G, Lopes A, Rossi BM, Ashton-Prolla P, Giugliani R, Palmero EI, Vargas FR, Da Rocha JC, Vettore AL, Hainaut P.
    Cancer Lett; 2007 Jan 08; 245(1-2):96-102. PubMed ID: 16494995
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  • 35. A chronic myeloid leukemia-like syndrome case with del (12) (p12) in a Li-Fraumeni syndrome family.
    Guran S, Beyan C, Nevruz O, Yakicier C, Tunca Y.
    Clin Lab Haematol; 2005 Apr 08; 27(2):135-8. PubMed ID: 15784129
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  • 36. Elevated frequency and functional activity of a specific germ-line p53 intron mutation in familial breast cancer.
    Lehman TA, Haffty BG, Carbone CJ, Bishop LR, Gumbs AA, Krishnan S, Shields PG, Modali R, Turner BC.
    Cancer Res; 2000 Feb 15; 60(4):1062-9. PubMed ID: 10706125
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  • 37. A method for estimating cancer risk in p53 mutation carriers.
    Le Bihan C, Bonaiti-Pellie C.
    Cancer Detect Prev; 1994 Feb 15; 18(3):171-8. PubMed ID: 8076379
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  • 38. [Hereditary mutations in the p53 tumor suppressor gene; significance for clinical practice. National Work Group Hereditary Mamma Carcinoma].
    Menko FH, Nooy MA, Vasen HF.
    Ned Tijdschr Geneeskd; 1996 Jun 29; 140(26):1347-50. PubMed ID: 8710022
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  • 40. 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 29; 98(2):156-9. PubMed ID: 16929790
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