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Journal Abstract Search

174 related items for PubMed ID: 17823852

  • 1. Loss of heterozygosity at 19p13.2 and 2q21 in tumours from familial clusters of non-medullary thyroid carcinoma.
    Prazeres HJ, Rodrigues F, Soares P, Naidenov P, Figueiredo P, Campos B, Lacerda M, Martins TC.
    Fam Cancer; 2008; 7(2):141-9. PubMed ID: 17823852
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  • 2. Familial non-medullary thyroid carcinoma (FNMTC): analysis of fPTC/PRN, NMTC1, MNG1 and TCO susceptibility loci and identification of somatic BRAF and RAS mutations.
    Cavaco BM, Batista PF, Martins C, Banito A, do Rosário F, Limbert E, Sobrinho LG, Leite V.
    Endocr Relat Cancer; 2008 Mar; 15(1):207-15. PubMed ID: 18310288
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  • 8. High-resolution 19p13.2-13.3 allelotyping of breast carcinomas demonstrates frequent loss of heterozygosity.
    Yang TL, Su YR, Huang CS, Yu JC, Lo YL, Wu PE, Shen CY.
    Genes Chromosomes Cancer; 2004 Nov; 41(3):250-6. PubMed ID: 15334548
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  • 12. The FOXE1 locus is a major genetic determinant for familial nonmedullary thyroid carcinoma.
    Bonora E, Rizzato C, Diquigiovanni C, Oudot-Mellakh T, Campa D, Vargiolu M, Guedj M, NMTC Consortium, McKay JD, Romeo G, Canzian F, Lesueur F.
    Int J Cancer; 2014 May 01; 134(9):2098-107. PubMed ID: 24127282
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  • 18. Multiple endocrine neoplasia type 1 (MEN1): LOH studies in a affected family and in sporadic cases.
    Valdes N, Alvarez V, Diaz-Cadorniga F, Aller J, Villazon F, Garcia I, Herrero A, Coto E.
    Anticancer Res; 1998 May 01; 18(4A):2685-9. PubMed ID: 9703929
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