Gösterilen 241 - 260 sonuçlar arası kayıtlar. 2,655 sonuç. Aranan kelime 'arm is (((((resolves. OR involves.) OR involves.) OR evolvedss.) OR involved.) OR resolve.)', Sorgu süresi: 0.45s Sonuçları Daraltın
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    Trialblazers: “Build-a-Trial” workshops for people with psoriatic arthritis Yazar: Caroline Struthers (754411)

    Baskı/Yayın Bilgisi 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. Yazar: Thibault Porssut (12184546)

    Baskı/Yayın Bilgisi 2022
    Konular:
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    The task. Yazar: Thibault Porssut (12184546)

    Baskı/Yayın Bilgisi 2022
    Konular:
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    Fig 1 - Yazar: Thibault Porssut (12184546)

    Baskı/Yayın Bilgisi 2022
    Konular:
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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... Yazar: Hulick P.J. (4121047)

    Baskı/Yayın Bilgisi 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... Yazar: Josef Davidsson (87327)

    Baskı/Yayın Bilgisi 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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