Torthaí cuardaigh - Lennart Raman

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  1. 1
    WisecondorX: improved copy number detection for routine shallow whole-genome sequencing

    WisecondorX: improved copy number detection for routine shallow whole-genome sequencing de réir Lennart Raman, Annelies Dheedene, Matthias De Smet, Jo Van Dorpe, Björn Menten

    Foilsithe / Cruthaithe 2018
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    Artigo
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  2. 2
    Shallow whole-genome sequencing of plasma cell-free DNA accurately differentiates small from non-small cell lung carcinoma

    Shallow whole-genome sequencing of plasma cell-free DNA accurately differentiates small from non-small cell lung carcinoma de réir Lennart Raman, Malaïka Van Der Linden, Kim Van der Eecken, Karim Vermaelen, Ingel Demedts, Veerle Surmont, Ulrike Himpe, Franceska Dedeurwaerdere, Liesbeth Ferdinande, Yolande Lievens, Kathleen Claes, Björn Menten, Jo Van Dorpe

    Foilsithe / Cruthaithe 2020
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    Artigo
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  3. 3
    Myxoid pleomorphic liposarcoma—a clinicopathologic, immunohistochemical, molecular genetic and epigenetic study of 12 cases, suggesting a possible relationship with conventional pleomorphic liposarcoma

    Myxoid pleomorphic liposarcoma—a clinicopathologic, immunohistochemical, molecular genetic and epigenetic study of 12 cases, suggesting a possible relationship with conventional pl... de réir David Creytens, Andrew L. Folpe, Christian Koelsche, Thomas Mentzel, Liesbeth Ferdinande, Joost M. van Gorp, Malaïka Van Der Linden, Lennart Raman, Björn Menten, Karen Fritchie, Andreas von Deimling, Jo Van Dorpe, Uta Flucke

    Foilsithe / Cruthaithe 2021
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    Artigo
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