Hasil Pencarian - Hopper J

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  1. 1
    P20-03. Identification of low frequency genetic variants during acute and early infection by parallel-allele specific sequencing

    P20-03. Identification of low frequency genetic variants during acute and early infection by parallel-allele specific sequencing oleh Kirchherr J, Hopper J, Chen S, Pavlicek JW, Gao F

    Diterbitkan 2009-10-01
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  2. 2
    Colorectal tumour BRAF V600E and MLH1 promoter methylation status in the assessment of mismatch repair gene sequence variants of unknown clinical significance

    Colorectal tumour BRAF V600E and MLH1 promoter methylation status in the assessment of mismatch repair gene sequence variants of unknown clinical significance oleh Parsons M, Thompson B, Goldgar D, Hopper J, Jenkins M, Buchanan D, Young J, Spurdle A

    Diterbitkan 2012-04-01
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  3. 3
    ‘Next-generation’ genome wide association studies

    ‘Next-generation’ genome wide association studies oleh Hopper J, Makalic E, Schmidt D, Bui M, Stone J, Kapuscinski M, Park D, Jenkins M, Southey M

    Diterbitkan 2012-04-01
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  4. 4
    P20-17. Evolution of multiple transmitted viruses during the early stage of HIV-1 infection

    P20-17. Evolution of multiple transmitted viruses during the early stage of HIV-1 infection oleh McMichael A, Goonetilleke N, Keele B, Pavlicek J, Chen S, Hopper J, Kirchherr JL, Haynes BF, Gao F

    Diterbitkan 2009-10-01
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  5. 5
    Validation study of risk prediction models for female relatives of Australian women with breast cancer

    Validation study of risk prediction models for female relatives of Australian women with breast cancer oleh MacInnis R, Dite G, Bickerstaffe A, Dowty J, Aujard K, Apicella C, Phillips K, Weideman P, Hopper J

    Diterbitkan 2012-04-01
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  6. 6
    Estimation of probabilities in favour of pathogenicity for missense substitutions for use in clinical evaluation of mismatch repair gene variants

    Estimation of probabilities in favour of pathogenicity for missense substitutions for use in clinical evaluation of mismatch repair gene variants oleh Thompson B, Goldgar D, Paterson C, Clendenning M, Walters R, Arnold S, Parsons M, Walsh M, Hopper J, Jenkins M, Greenblatt M, Buchanan D, Young J, Tavtigian S, Spurdle A

    Diterbitkan 2012-04-01
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  7. 7
    From GWAS to genome sequencing: complementary approaches to identify melanoma predisposition genes

    From GWAS to genome sequencing: complementary approaches to identify melanoma predisposition genes oleh MacGregor S, Brown KM, Stark M, Gartside M, Woods S, Bonazzi V, Aoude L, Dutton-Regester K, Tyagi S, Liu J, Duffy DL, Palmer J, Cust A, Schmid H, Symmons J, Holland E, Agha-Hamilton C, Holohan K, Youngkin D, Gillanders E, Jenkins MA, Kelly J, Whiteman DC, Kefford R, Giles G, Armstrong B, Aitken J, Hopper J, Montgomery G, Schmidt C, Trent JM, Martin NG, Mann GJ, Hayward NK

    Diterbitkan 2012-04-01
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