Search Results - Taylor, Sherryl A.M.

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  1. 1
    Quantitative neuropathological changes in presymptomatic Huntington's disease

    Quantitative neuropathological changes in presymptomatic Huntington's disease by Gómez-Tortosa, Estrella, MacDonald, Marcy E., Friend, Julia C., Taylor, Sherryl A.M., Weiler, Larry J., Cupples, L. Adrienne, Srinidhi, Jayalakshmi, Gusella, James F., Bird, Edward D., Vonsattel, Jean-Paul, Myers, Richard H.

    Published in Annals of neurology
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  2. 2
    Paternal transmission of fragile X syndrome

    Paternal transmission of fragile X syndrome by Zeesman, Susan, Zwaigenbaum, Lonnie, Whelan, Donald T., Hagerman, Randi J., Tassone, Flora, Taylor, Sherryl A.M.

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  3. 3
    Boy with 47,XXY,del(15)(q11.2q13) karyotype and Prader–Willi syndrome: A new case and review of the literature

    Boy with 47,XXY,del(15)(q11.2q13) karyotype and Prader–Willi syndrome: A new case and review of the literature by Nowaczyk, Małgorzata J.M., Zeesman, Susan, Kam, April, Taylor, Sherryl A.M., Carter, Ronald F., Whelan, Donald T.

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  4. 4
    No evidence of paternal transmission of fragile X syndrome

    No evidence of paternal transmission of fragile X syndrome by Steinbach, Doris, Steinbach, Peter

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  5. 5
    Response to letter: "No evidence of paternal transmission of fragile X syndrome" by Doris and Peter Steinbach

    Response to letter: "No evidence of paternal transmission of fragile X syndrome" by Doris and Peter Steinbach by Tassone, Flora, Zeesman, Susan, Zwaigenbaum, Lonnie, Whelan, Donald T., Hagerman, Randi J., Taylor, Sherryl A.M.

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  6. 6
    Risk of venous thromboembolism associated with the common hereditary haemochromatosis Hfe gene (C282Y) mutation

    Risk of venous thromboembolism associated with the common hereditary haemochromatosis Hfe gene (C282Y) mutation by Brown, Karen, Luddington, Roger, Taylor, Sherryl A. M., Lillicrap, David P., Baglin, Trevor P.

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  7. 7
    Direct Detection of a Common Inversion Mutation in the Genetic Diagnosis of Severe Hemophilia A

    Direct Detection of a Common Inversion Mutation in the Genetic Diagnosis of Severe Hemophilia A by Windsor, Sharon, Taylor, Sherryl A.M., Lillicrap, David

    Published in Blood
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  8. 8
    Direct detection of a common inversion mutation in the genetic diagnosis of severe hemophilia A [see comments]

    Direct detection of a common inversion mutation in the genetic diagnosis of severe hemophilia A [see comments] by Windsor, S, Taylor, SA, Lillicrap, D

    Published in Blood
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  9. 9
    Mutation of RET codon 768 is associated with the FMTC phenotype

    Mutation of RET codon 768 is associated with the FMTC phenotype by Boccia, Lara M., Green, Jane S., Joyce, Carol, Eng, Charts, Taylor, Sherryl A. M., Mulligan, Lois M.

    Published in Clinical genetics
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  10. 10
    A gene from chromosome 4p 16.3 with similarity to a superfamily of transporter proteins

    A gene from chromosome 4p 16.3 with similarity to a superfamily of transporter proteins by Duyao, Mabel P., Taylor, Sherryl A.M., Buckler, Alan J., Ambrose, Christine M., Lin, Carol, Groot, Nicolet, Church, Deanna, Barnes, Glenn, Wasmuth, John J., Housman, David E., MacDonald, Marcy E., Gusella, James F.

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  11. 11
    Paternal transmission of fragile X syndrome

    Paternal transmission of fragile X syndrome by Zeesman, Susan, Zwaigenbaum, Lonnie, Whelan, Donald T., Hagerman, Randi J., Tassone, Flora, Taylor, Sherryl A.M.

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  12. 12
    Boy with 47,XXY,del(15)(q11.2q13) karyotype and Prader-Willi syndrome: A new case and review of the literature

    Boy with 47,XXY,del(15)(q11.2q13) karyotype and Prader-Willi syndrome: A new case and review of the literature by Nowaczyk, Małgorzata J.M., Zeesman, Susan, Kam, April, Taylor, Sherryl A.M., Carter, Ronald F., Whelan, Donald T.

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