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Journal Abstract Search

168 related items for PubMed ID: 16174859

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  • 3. Genome-wide search for nevus density shows linkage to two melanoma loci on chromosome 9 and identifies a new QTL on 5q31 in an adult twin cohort.
    Falchi M, Spector TD, Perks U, Kato BS, Bataille V.
    Hum Mol Genet; 2006 Oct 15; 15(20):2975-9. PubMed ID: 16928783
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  • 6. Mapping the gene for hereditary cutaneous malignant melanoma-dysplastic nevus to chromosome 1p.
    Bale SJ, Dracopoli NC, Tucker MA, Clark WH, Fraser MC, Stanger BZ, Green P, Donis-Keller H, Housman DE, Greene MH.
    N Engl J Med; 1989 May 25; 320(21):1367-72. PubMed ID: 2716782
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  • 7. Deletion mapping suggests that the 1p22 melanoma susceptibility gene is a tumor suppressor localized to a 9-Mb interval.
    Walker GJ, Indsto JO, Sood R, Faruque MU, Hu P, Pollock PM, Duray P, Holland EA, Brown K, Kefford RF, Trent JM, Mann GJ, Hayward NK.
    Genes Chromosomes Cancer; 2004 Sep 25; 41(1):56-64. PubMed ID: 15236317
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  • 9. Linkage analysis in Dutch familial atypical multiple mole-melanoma (FAMMM) syndrome families. Effect of naevus count.
    Gruis NA, Sandkuijl LA, Weber JL, van der Zee A, Borgstein AM, Bergman W, Frants RR.
    Melanoma Res; 1993 Aug 25; 3(4):271-7. PubMed ID: 8219760
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  • 12. A large Norwegian family with inherited malignant melanoma, multiple atypical nevi, and CDK4 mutation.
    Molven A, Grimstvedt MB, Steine SJ, Harland M, Avril MF, Hayward NK, Akslen LA.
    Genes Chromosomes Cancer; 2005 Sep 25; 44(1):10-8. PubMed ID: 15880589
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  • 14. A narcolepsy susceptibility locus maps to a 5 Mb region of chromosome 21q.
    Dauvilliers Y, Blouin JL, Neidhart E, Carlander B, Eliaou JF, Antonarakis SE, Billiard M, Tafti M.
    Ann Neurol; 2004 Sep 25; 56(3):382-8. PubMed ID: 15349865
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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 25; 12(2):98-104. PubMed ID: 14560309
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  • 16. Investigation of a putative melanoma susceptibility locus at chromosome 3q29.
    Tuominen R, Jönsson G, Enerbäck C, Appelqvist F, Olsson H, Ingvar C, Hansson J, Höiom V.
    Cancer Genet; 2014 Mar 25; 207(3):70-4. PubMed ID: 24721441
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  • 17. Linkage analysis of extended high-risk pedigrees replicates a cutaneous malignant melanoma predisposition locus on chromosome 9q21.
    Cannon-Albright LA, Teerlink CC, Farnham JM, Thomas AW, Zone JJ, Leachman SA.
    J Invest Dermatol; 2013 Jan 25; 133(1):128-34. PubMed ID: 22951724
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  • 18. Analysis of mutations in the p16/CDKN2A gene in sporadic and familial melanoma in the Polish population.
    Lamperska K, Karezewska A, Kwiatkowska E, Mackiewicz A.
    Acta Biochim Pol; 2002 Jan 25; 49(2):369-76. PubMed ID: 12362978
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  • 19. Objective prioritization of positional candidate genes at a quantitative trait locus for pre-eclampsia on 2q22.
    Moses EK, Fitzpatrick E, Freed KA, Dyer TD, Forrest S, Elliott K, Johnson MP, Blangero J, Brennecke SP.
    Mol Hum Reprod; 2006 Aug 25; 12(8):505-12. PubMed ID: 16809377
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  • 20. Molecular characterization of a t(9;12)(p21;q13) balanced chromosome translocation in combination with integrative genomics analysis identifies C9orf14 as a candidate tumor-suppressor.
    Pujana MA, Ruiz A, Badenas C, Puig-Butille JA, Nadal M, Stark M, Gómez L, Valls J, Solé X, Hernández P, Cerrato C, Madrigal I, de Cid R, Aguilar H, Capellá G, Cal S, James MR, Walker GJ, Malvehy J, Milà M, Hayward NK, Estivill X, Puig S.
    Genes Chromosomes Cancer; 2007 Feb 25; 46(2):155-62. PubMed ID: 17099875
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