Čájehuvvojit 241 - 260 oktiibuot 2 655 bohtosis ohcui arm is (((((resolves. OR involves.) OR involves.) OR evolvedss.) OR involved.) OR resolved.)', ohcanáigi: 1,34s Aiddostahte ozu
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    Trialblazers: “Build-a-Trial” workshops for people with psoriatic arthritis Dahkki Caroline Struthers (754411)

    Almmustuhtton 2024
    “…This was to be followed in June 2024 by an application to the Medical Research Council (MRC) funding stream for a grant in understanding public involvement in non-clinical research.</p><p dir="ltr">In collaboration with the NDORMS’ public-involvement group, Open Arms, and led by clinician researcher Laura Coates, the team developed and ran Build-a-Trial workshops with patients to design this much needed trial from scratch. …”
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    Protocol overview. Dahkki Thibault Porssut (12184546)

    Almmustuhtton 2022
    Fáttát:
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    The task. Dahkki Thibault Porssut (12184546)

    Almmustuhtton 2022
    Fáttát:
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    Fig 1 - Dahkki Thibault Porssut (12184546)

    Almmustuhtton 2022
    Fáttát:
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    Supplementary Material for: Cytogenetic and Array-CGH Characterization of a Complex de novo Rearrangement Involving Duplication and Deletion of 9p and Clinical Findings in a 4-Mont... Dahkki Hulick P.J. (4121047)

    Almmustuhtton 2010
    “…Here, we present clinical, cytogenetic, FISH and aCGH findings in a patient with a de novo complex rearrangement in the short arm of chromosome 9 involving an inverted duplication at 9p24→p21.3 and a deletion at 9pter→p24.2. …”
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    Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental... Dahkki Josef Davidsson (87327)

    Almmustuhtton 2011
    “…<p><b>Copyright information:</b></p><p>Taken from "Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay"</p><p>http://www.biomedcentral.com/1471-2350/9/2</p><p>BMC Medical Genetics 2008;9():2-2.…”
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