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Journal Abstract Search

220 related items for PubMed ID: 8221639

  • 1. Linkage analysis of DRD2, a marker linked to the ataxia-telangiectasia gene, in 64 families with premenopausal bilateral breast cancer.
    Cortessis V, Ingles S, Millikan R, Diep A, Gatti RA, Richardson L, Thompson WD, Paganini-Hill A, Sparkes RS, Haile RW.
    Cancer Res; 1993 Nov 01; 53(21):5083-6. PubMed ID: 8221639
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  • 7. Familial male breast cancer is not linked to the BRCA1 locus on chromosome 17q.
    Stratton MR, Ford D, Neuhasen S, Seal S, Wooster R, Friedman LS, King MC, Egilsson V, Devilee P, McManus R.
    Nat Genet; 1994 May 01; 7(1):103-7. PubMed ID: 8075631
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  • 8. [Hereditary predisposition for cancer of the breast and the ovary].
    Lalle P, Stoppa-Lyonnet D, Mazoyer S, Rio P, Girodet C, Hardouin A, Narod SA, Sobol H, Bignon YJ.
    Bull Cancer; 1993 Oct 01; 80(10):857-65. PubMed ID: 8204923
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  • 12. A physical map across chromosome 11q22-q23 containing the major locus for ataxia telangiectasia.
    Ambrose HJ, Byrd PJ, McConville CM, Cooper PR, Stankovic T, Riley JH, Shiloh Y, McNamara JO, Fukao T, Taylor AM.
    Genomics; 1994 Jun 01; 21(3):612-9. PubMed ID: 7959739
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  • 13. Linkage analysis and loss of heterozygosity for chromosome arm 1p in familial breast cancer.
    Millikan RC, Ingles SA, Diep AT, Xue S, Zhou N, Florentine BD, Sparkes RS, Haile RW.
    Genes Chromosomes Cancer; 1999 Aug 01; 25(4):354-61. PubMed ID: 10398429
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  • 14. Skewed X chromosome inactivation and breast and ovarian cancer status: evidence for X-linked modifiers of BRCA1.
    Lose F, Duffy DL, Kay GF, Kedda MA, Spurdle AB, Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer, Australian Ovarian Cancer Study Management Group.
    J Natl Cancer Inst; 2008 Nov 05; 100(21):1519-29. PubMed ID: 18957670
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  • 15. Genome-wide scanning for linkage in Finnish breast cancer families.
    Huusko P, Juo SH, Gillanders E, Sarantaus L, Kainu T, Vahteristo P, Allinen M, Jones M, Rapakko K, Eerola H, Markey C, Vehmanen P, Gildea D, Freas-Lutz D, Blomqvist C, Leisti J, Blanco G, Puistola U, Trent J, Bailey-Wilson J, Winqvist R, Nevanlinna H, Kallioniemi OP.
    Eur J Hum Genet; 2004 Feb 05; 12(2):98-104. PubMed ID: 14560309
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  • 16. DNA screening for breast/ovarian cancer susceptibility based on linked markers. A family study.
    Lynch HT, Watson P, Conway TA, Lynch JF, Slominski-Caster SM, Narod SA, Feunteun J, Lenoir G.
    Arch Intern Med; 1993 Sep 13; 153(17):1979-87. PubMed ID: 8357282
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  • 17. Analysis of breast cancer pedigrees using affected sibship methods.
    Barrett JH, Rigby AS.
    Genet Epidemiol; 1995 Sep 13; 12(6):847-51. PubMed ID: 8788020
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  • 18. Mutation analysis and characterization of ATR sequence variants in breast cancer cases from high-risk French Canadian breast/ovarian cancer families.
    Durocher F, Labrie Y, Soucy P, Sinilnikova O, Labuda D, Bessette P, Chiquette J, Laframboise R, Lépine J, Lespérance B, Ouellette G, Pichette R, Plante M, Tavtigian SV, Simard J.
    BMC Cancer; 2006 Sep 29; 6():230. PubMed ID: 17010193
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  • 19. Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus.
    Phelan CM, Rebbeck TR, Weber BL, Devilee P, Ruttledge MH, Lynch HT, Lenoir GM, Stratton MR, Easton DF, Ponder BA, Cannon-Albright L, Larsson C, Goldgar DE, Narod SA.
    Nat Genet; 1996 Mar 29; 12(3):309-11. PubMed ID: 8589723
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  • 20. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW, Lee DD, Lin CH, Huang CY, Wong CK, Chang YT, Liu HN, Hsiao KJ, Tsai SF.
    Br J Dermatol; 2005 Jan 29; 152(1):29-36. PubMed ID: 15656797
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