Rezultati - Diane Wilson

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  1. 1
    Transmission of Z allele from heterozygotes for α1-antitrypsin deficiency

    Transmission of Z allele from heterozygotes for α1-antitrypsin deficiency od Cox, Diane Wilson

    Izdano 1980
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  2. 2
    Investigation of Possible Genetic Damage in the Offspring of Women Receiving Multiple Diagnostic Pelvic X rays

    Investigation of Possible Genetic Damage in the Offspring of Women Receiving Multiple Diagnostic Pelvic X rays od Cox, Diane Wilson

    Izdano 1964
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  3. 3
    A Screening Test for Wilson's Disease and its Application to Psychiatric Patients

    A Screening Test for Wilson's Disease and its Application to Psychiatric Patients od Cox, Diane Wilson

    Izdano 1967
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  4. 4
    Trasicor in Angina Pectoris: a Double-blind Trial

    Trasicor in Angina Pectoris: a Double-blind Trial od Diane Wilson, Olwen F. Watson, J. S. Peel, A. S. Turner

    Izdano 1969
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  5. 5
    A genetic study of Wilson's disease: Evidence for heterogeneity

    A genetic study of Wilson's disease: Evidence for heterogeneity od Cox, Diane Wilson, Fraser, F. Clarke, Sass-Kortsak, Andrew

    Izdano 1972
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  6. 6
    CHOICE MAKING TO PROMOTE ADAPTIVE BEHAVIOR FOR STUDENTS WITH EMOTIONAL AND BEHAVIORAL CHALLENGES

    CHOICE MAKING TO PROMOTE ADAPTIVE BEHAVIOR FOR STUDENTS WITH EMOTIONAL AND BEHAVIORAL CHALLENGES od Glen Dunlap, Maria dePerczel, Shelley Clarke, Diane Wilson, Suzanne Wright, Ronnie White, Arcadia Gomez

    Izdano 1994
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  7. 7
    Who Goes First? Influences of Human-AI Workflow on Decision Making in Clinical Imaging

    Who Goes First? Influences of Human-AI Workflow on Decision Making in Clinical Imaging od Riccardo Fogliato, Shreya Chappidi, Matthew P. Lungren, Paul Fisher, Diane Wilson, Michael Fitzke, Mark Parkinson, Eric Horvitz, Kori Inkpen, Besmira Nushi

    Izdano 2022
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  8. 8
    Prospective cohort study for identification of underlying genetic causes in neonatal encephalopathy using whole-exome sequencing

    Prospective cohort study for identification of underlying genetic causes in neonatal encephalopathy using whole-exome sequencing od Theodora U. J. Bruun, Caro-Lyne DesRoches, Diane Wilson, Vann Chau, Tadashi Nakagawa, Masahiro Yamasaki, Shinya Hasegawa, Toshiyuki Fukao, Christian R. Marshall, Saadet Mercimek‐Andrews

    Izdano 2017
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