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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 由 D. Williams Parsons

    出版 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 由 Carl E. Allen, D. Williams Parsons

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

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

    出版 2010
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  4. 4
    Precision Medicine in Pediatric Oncology

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

    出版 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 由 Seymour B. Koritz, Fernand G. Péron, D. Williams Parsons

    出版 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 由 Fernand G. Péron, Seymour B. Koritz, D. Williams Parsons

    出版 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 由 Hai Yan, Darell D. Bigner, Victor E. Velculescu, D. Williams Parsons

    出版 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 由 Avadhut D. Joshi, D. Williams Parsons, Victor E. Velculescu, Gregory J. Riggins

    出版 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 由 Rajen Mody, John R. Prensner, Jessica N. Everett, D. Williams Parsons, Arul M. Chinnaiyan

    出版 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 由 D. Williams Parsons, Patricia McAndrew, ST Iannaccone, Jerry R. Mendell, Arthur H.M. Burghes, T. Prior

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

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

    出版 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. 由 Victoria M. Raymond, Stacy W. Gray, Sameek Roychowdhury, Steven Joffe, Arul M. Chinnaiyan, D. Williams Parsons, Sharon E. Plon

    出版 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 由 Patricia McAndrew, D. Williams Parsons, Louise R. Simard, Camille Rochette, Peter N. Ray, Jerry R. Mendell, Thomas W. Prior, Arthur H.M. Burghes

    出版 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 由 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

    出版 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 由 Janet Malek, Melody J. Slashinski, Jill O. Robinson, Amanda M. Gutierrez, D. Williams Parsons, Sharon E. Plon, Laurence B. McCullough, Amy L. McGuire

    出版 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 由 Laurence B. McCullough, Melody J. Slashinski, Amy L. McGuire, Richard L. Street, Christine M. Eng, Richard A. Gibbs, D. Williams Parsons, Sharon E. Plon

    出版 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 由 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

    出版 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 由 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

    出版 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 由 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

    出版 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 由 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

    出版 2014
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