Search Results - Rogan, P.K.

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  1. 1
    Imprinting-Mutation Mechanisms in Prader-Willi Syndrome

    Imprinting-Mutation Mechanisms in Prader-Willi Syndrome by Ohta, T., Gray, T.A., Rogan, P.K., Buiting, K., Gabriel, J.M., Saitoh, S., Muralidhar, B., Bilienska, B., Krajewska-Walasek, M., Driscoll, D.J., Horsthemke, B., Butler, M.G., Nicholls, R.D.

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  2. 2
    Survival outcome differences based on treatments used and knowledge of the primary tumour site for patients with cancer of unknown and known primary in Ontario

    Survival outcome differences based on treatments used and knowledge of the primary tumour site for patients with cancer of unknown and known primary in Ontario by Kim, C S, Hannouf, M B, Sarma, S, Rodrigues, G B, Rogan, P K, Mahmud, S M, Winquist, E, Brackstone, M, Zaric, G S

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  3. 3
    The clinical significance of occult gynecologic primary tumours in metastatic cancer

    The clinical significance of occult gynecologic primary tumours in metastatic cancer by Hannouf, M B, Winquist, E, Mahmud, S M, Brackstone, M, Sarma, S, Rodrigues, G, Rogan, P K, Hoch, J S, Zaric, G S

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  4. 4
    Characterization of an African American (AA) subject carrying two novel functional CYP2D6 alleles

    Characterization of an African American (AA) subject carrying two novel functional CYP2D6 alleles by Gaedigk, A., Abdel‐Rahman, S.M., Marcucci, K.A., Pearce, R.E., Rogan, P.K., Bradford, L.D., Spielberg, S.P., Leeder, J.S.

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  5. 5
    Ab initio exon definition using an information theory-based approach

    Ab initio exon definition using an information theory-based approach by Rogan, P.K.

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  6. 6
    Bloom syndrome and maternal uniparental disomy for chromosome 15

    Bloom syndrome and maternal uniparental disomy for chromosome 15 by WOODAGE, T, MADHURI PRASAD, TRENT, R. J, DIXON, J. W, SELBY, R. E, ROMAIN, D. R, COLUMBANO-GREEN, L. M, GRAHAM, D, ROGAN, P. K, SEIP, J. R, SMITH, A

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  7. 7
    A common insertion/deletion polymorphism in the Prader—Willi syndrome minimal critical region

    A common insertion/deletion polymorphism in the Prader—Willi syndrome minimal critical region by Gabriel, J., Gottlieb, W., Garcia, A., Rogan, P.K., Saitoh, S., Nicholls, R.D.

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  8. 8
    A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy

    A new missense mutation, Arg719Gln, in the β-cardiac heavy chain myosin gene of patients with familial hypertrophic cardiomyopathy by Consevage, M.W., Salada, G.C., Baylen, B.G., Ladda, R.L., Rogan, P.K.

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  9. 9
    Phylogenetic inference based on information theory-based PCR amplification

    Phylogenetic inference based on information theory-based PCR amplification by Tooley, P.W, Salvo, J.J, Schneider, T.D, Rogan, P.K

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  10. 10
    High resolution detection of chromosome abnormalities with single copy fluorescence in situ hybridization

    High resolution detection of chromosome abnormalities with single copy fluorescence in situ hybridization by Rogan, P.K., Knoll, J.H.M.

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