Search Results - "Dougherty, Margaret J"

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  1. 1

    Activating mutations in BRAF characterize a spectrum of pediatric low-grade gliomas by Dougherty, Margaret J., Santi, Mariarita, Brose, Marcia S., Ma, Changqing, Resnick, Adam C., Sievert, Angela J., Storm, Phillip B., Biegel, Jaclyn A.

    Published in Neuro-oncology (Charlottesville, Va.) (01-07-2010)
    “…In the present study, DNA from 27 grade I and grade II pediatric gliomas, including ganglioglioma, desmoplastic infantile ganglioglioma, dysembryoplastic…”
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    Journal Article
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    Temporal lobe pleomorphic xanthoastrocytoma and acquired BRAF mutation in an adolescent with the constitutional 22q11.2 deletion syndrome by Murray, Jeffrey C., Donahue, David J., Malik, Saleem I., Dzurik, Yvette B., Braly, Emily Z., Dougherty, Margaret J., Eaton, Katherine W., Biegel, Jaclyn A.

    Published in Journal of neuro-oncology (01-05-2011)
    “…DiGeorge syndrome, or velocardiofacial syndrome (DGS/VCFS), is a rare and usually sporadic congenital genetic disorder resulting from a constitutional…”
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    Journal Article
  4. 4

    Implementation of high resolution single nucleotide polymorphism array analysis as a clinical test for patients with hematologic malignancies by Dougherty, Margaret J, Wilmoth, Donna M, Tooke, Laura S, Shaikh, Tamim H, Gai, Xiaowu, Hakonarson, Hakon, Biegel, Jaclyn A

    Published in Cancer genetics (2011)
    “…Single nucleotide polymorphism–based oligonucleotide arrays have been used as a research tool to detect genomic copy number changes and allelic imbalance in a…”
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    Journal Article
  5. 5

    Clinical utilization of high-resolution single nucleotide polymorphism based oligonucleotide arrays in diagnostic studies of pediatric patients with solid tumors by Dougherty, Margaret J, Tooke, Laura S, Sullivan, Lisa M, Hakonarson, Hakon, Wainwright, Luanne M, Biegel, Jaclyn A

    Published in Cancer genetics (01-01-2012)
    “…High-resolution single nucleotide polymorphism (SNP) arrays have been effectively implemented as a first tier test in clinical cytogenetics laboratories for…”
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    Journal Article