Canlyniadau Chwilio - D. Williams Parsons

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  1. 1
    An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene

    An 11 base pair duplication in exon 6 of the SMN gene produces a type I spinal muscular atrophy (SMA) phenotype: further evidence for SMN as the primary SMA-determining gene gan D. Williams Parsons

    Cyhoeddwyd 1996
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  2. 2
    Biological and clinical significance of somatic mutations in Langerhans cell histiocytosis and related histiocytic neoplastic disorders

    Biological and clinical significance of somatic mutations in Langerhans cell histiocytosis and related histiocytic neoplastic disorders gan Carl E. Allen, D. Williams Parsons

    Cyhoeddwyd 2015
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  3. 3
    IDH1 and IDH2: Not Your Typical Oncogenes

    IDH1 and IDH2: Not Your Typical Oncogenes gan Zachary J. Reitman, D. Williams Parsons, Hai Yan

    Cyhoeddwyd 2010
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  4. 4
    Precision Medicine in Pediatric Oncology

    Precision Medicine in Pediatric Oncology gan Kieuhoa T. Vo, D. Williams Parsons, Nita L. Seibel

    Cyhoeddwyd 2019
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  5. 5
    STUDIES ON THE MODE OF ACTION OF THE ADRENOCORTICOTROPIC HORMONE

    STUDIES ON THE MODE OF ACTION OF THE ADRENOCORTICOTROPIC HORMONE gan Seymour B. Koritz, Fernand G. Péron, D. Williams Parsons

    Cyhoeddwyd 1958
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  6. 6
    On the Exogenous Requirements for the Action of ACTH in Vitro on Rat Adrenal Glands

    On the Exogenous Requirements for the Action of ACTH in Vitro on Rat Adrenal Glands gan Fernand G. Péron, Seymour B. Koritz, D. Williams Parsons

    Cyhoeddwyd 1958
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  7. 7
    Mutant Metabolic Enzymes Are at the Origin of Gliomas

    Mutant Metabolic Enzymes Are at the Origin of Gliomas gan Hai Yan, Darell D. Bigner, Victor E. Velculescu, D. Williams Parsons

    Cyhoeddwyd 2009
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  8. 8
    Sodium ion channel mutations in glioblastoma patients correlate with shorter survival

    Sodium ion channel mutations in glioblastoma patients correlate with shorter survival gan Avadhut D. Joshi, D. Williams Parsons, Victor E. Velculescu, Gregory J. Riggins

    Cyhoeddwyd 2011
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  9. 9
    Precision medicine in pediatric oncology: Lessons learned and next steps

    Precision medicine in pediatric oncology: Lessons learned and next steps gan Rajen Mody, John R. Prensner, Jessica N. Everett, D. Williams Parsons, Arul M. Chinnaiyan

    Cyhoeddwyd 2016
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  10. 10
    Intragenic telSMN Mutations: Frequency, Distribution, Evidence of a Founder Effect, and Modification of the Spinal Muscular Atrophy Phenotype by cenSMN Copy Number

    Intragenic telSMN Mutations: Frequency, Distribution, Evidence of a Founder Effect, and Modification of the Spinal Muscular Atrophy Phenotype by cenSMN Copy Number gan D. Williams Parsons, Patricia McAndrew, ST Iannaccone, Jerry R. Mendell, Arthur H.M. Burghes, T. Prior

    Cyhoeddwyd 1998
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  11. 11
    Epitope Landscape in Breast and Colorectal Cancer

    Epitope Landscape in Breast and Colorectal Cancer gan Neil H. Segal, D. Williams Parsons, Karl S. Peggs, Victor E. Velculescu, Ken W Kinzler, Bert Vogelstein, James P. Allison

    Cyhoeddwyd 2008
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  12. 12
    Germline Findings in Tumor-Only Sequencing: Points to Consider for Clinicians and Laboratories: Table 1.

    Germline Findings in Tumor-Only Sequencing: Points to Consider for Clinicians and Laboratories: Table 1. gan Victoria M. Raymond, Stacy W. Gray, Sameek Roychowdhury, Steven Joffe, Arul M. Chinnaiyan, D. Williams Parsons, Sharon E. Plon

    Cyhoeddwyd 2015
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  13. 13
    Identification of Proximal Spinal Muscular Atrophy Carriers and Patients by Analysis of SMNT and SMNC Gene Copy Number

    Identification of Proximal Spinal Muscular Atrophy Carriers and Patients by Analysis of SMNT and SMNC Gene Copy Number gan Patricia McAndrew, D. Williams Parsons, Louise R. Simard, Camille Rochette, Peter N. Ray, Jerry R. Mendell, Thomas W. Prior, Arthur H.M. Burghes

    Cyhoeddwyd 1997
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  14. 14
    The Challenge of Informed Consent and Return of Results in Translational Genomics: Empirical Analysis and Recommendations

    The Challenge of Informed Consent and Return of Results in Translational Genomics: Empirical Analysis and Recommendations gan Gail E. Henderson, Susan M. Wolf, Kristine J. Kuczynski, Steven Joffe, Richard R. Sharp, D. Williams Parsons, Bartha Maria Knoppers, Joon‐Ho Yu, Paul S. Appelbaum

    Cyhoeddwyd 2014
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  15. 15
    Parental Perspectives on Whole-Exome Sequencing in Pediatric Cancer: A Typology of Perceived Utility

    Parental Perspectives on Whole-Exome Sequencing in Pediatric Cancer: A Typology of Perceived Utility gan Janet Malek, Melody J. Slashinski, Jill O. Robinson, Amanda M. Gutierrez, D. Williams Parsons, Sharon E. Plon, Laurence B. McCullough, Amy L. McGuire

    Cyhoeddwyd 2017
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  16. 16
    Is Whole-Exome Sequencing an Ethically Disruptive Technology? Perspectives of Pediatric Oncologists and Parents of Pediatric Patients With Solid Tumors

    Is Whole-Exome Sequencing an Ethically Disruptive Technology? Perspectives of Pediatric Oncologists and Parents of Pediatric Patients With Solid Tumors gan Laurence B. McCullough, Melody J. Slashinski, Amy L. McGuire, Richard L. Street, Christine M. Eng, Richard A. Gibbs, D. Williams Parsons, Sharon E. Plon

    Cyhoeddwyd 2015
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  17. 17
    Target and Agent Prioritization for the Children’s Oncology Group—National Cancer Institute Pediatric MATCH Trial

    Target and Agent Prioritization for the Children’s Oncology Group—National Cancer Institute Pediatric MATCH Trial gan Carl E. Allen, Theodore W. Laetsch, Rajen Mody, Meredith S. Irwin, Megan S. Lim, Peter C. Adamson, Nita L. Seibel, D. Williams Parsons, Y. Jae Cho, Katherine A. Janeway

    Cyhoeddwyd 2016
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  18. 18
    A multidimensional analysis of genes mutated in breast and colorectal cancers

    A multidimensional analysis of genes mutated in breast and colorectal cancers gan Jimmy Lin, Christine Gan, Xiaosong Zhang, Siân Jones, Tobias Sjöblom, Laura D. Wood, D. Williams Parsons, Nickolas Papadopoulos, Kenneth W. Kinzler, Bert Vogelstein, Giovanni Parmigiani, Victor E. Velculescu

    Cyhoeddwyd 2007
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  19. 19
    Reliable tumor detection by whole-genome methylation sequencing of cell-free DNA in cerebrospinal fluid of pediatric medulloblastoma

    Reliable tumor detection by whole-genome methylation sequencing of cell-free DNA in cerebrospinal fluid of pediatric medulloblastoma gan Jia Li, Sibo Zhao, Minjung Lee, Yue Yin, Jin Li, Yubin Zhou, Leomar Y. Ballester, Yoshua Esquenazi, Roderick H. Dashwood, Peter J. Davies, D. Williams Parsons, Xiao‐Nan Li, Yun Huang, Deqiang Sun

    Cyhoeddwyd 2020
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  20. 20
    Obtaining informed consent for clinical tumor and germline exome sequencing of newly diagnosed childhood cancer patients

    Obtaining informed consent for clinical tumor and germline exome sequencing of newly diagnosed childhood cancer patients gan Sarah Scollon, Katie Bergstrom, Robin A. Kerstein, Tao Wang, Susan G. Hilsenbeck, Uma Ramamurthy, Richard A. Gibbs, Christine M. Eng, Murali Chintagumpala, Stacey L. Berg, Laurence B. McCullough, Amy L. McGuire, Sharon E. Plon, D. Williams Parsons

    Cyhoeddwyd 2014
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