Hasil Pencarian - Aimée D C Paulussen

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  1. 1
    Next-Generation Sequencing in Oncology: Genetic Diagnosis, Risk Prediction and Cancer Classification

    Next-Generation Sequencing in Oncology: Genetic Diagnosis, Risk Prediction and Cancer Classification oleh Rick Kamps, Rita D. Brandão, Bianca J. van den Bosch, Aimee D. C. Paulussen, Sofia Xanthoulea, Marinus J. Blok, Andrea Romano

    Diterbitkan 2017-01-01
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  2. 2
    Erythrocyte inosine triphosphatase activity is decreased in HIV-seropositive individuals.

    Erythrocyte inosine triphosphatase activity is decreased in HIV-seropositive individuals. oleh Jörgen Bierau, Jaap A Bakker, Jolanda A Schippers, Janine A C Grashorn, Martijn Lindhout, Selwyn H Lowe, Aimée D C Paulussen, Annelies Verbon

    Diterbitkan 2012-01-01
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  3. 3
    Erythrocyte Inosine triphosphatase activity: A potential biomarker for adverse events during combination antiretroviral therapy for HIV.

    Erythrocyte Inosine triphosphatase activity: A potential biomarker for adverse events during combination antiretroviral therapy for HIV. oleh N Chantal Peltenburg, Jörgen Bierau, Jaap A Bakker, Jolanda A Schippers, Selwyn H Lowe, Aimée D C Paulussen, Bianca J C van den Bosch, Mathie P G Leers, Bettina E Hansen, Annelies Verbon

    Diterbitkan 2018-01-01
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  4. 4
    Detection of <i>PTCH1</i> Copy-Number Variants in Mosaic Basal Cell Nevus Syndrome

    Detection of <i>PTCH1</i> Copy-Number Variants in Mosaic Basal Cell Nevus Syndrome oleh Guido M. J. M. Roemen, Tom E. J. Theunissen, Ward W. J. Hoezen, Anja R. M. Steyls, Aimee D. C. Paulussen, Klara Mosterd, Elisa Rahikkala, Axel zur Hausen, Ernst Jan M. Speel, Michel van Geel

    Diterbitkan 2024-01-01
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  5. 5
    Evolution of Dihydropyrimidine Dehydrogenase Diagnostic Testing in a Single Center during an 8-Year Period of Time

    Evolution of Dihydropyrimidine Dehydrogenase Diagnostic Testing in a Single Center during an 8-Year Period of Time oleh Marieke J.H. Coenen, PhD, Aimée D.C. Paulussen, PhD, Marc Breuer, BSc, Martijn Lindhout, BSc, Demis C.J. Tserpelis, BSc, Anja Steyls, BSc, Jörgen Bierau, PhD, Bianca J.C. van den Bosch, PhD

    Diterbitkan 2019-01-01
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  6. 6
    Genome sequencing as a generic diagnostic strategy for rare disease

    Genome sequencing as a generic diagnostic strategy for rare disease oleh Gaby Schobers, Ronny Derks, Amber den Ouden, Hilde Swinkels, Jeroen van Reeuwijk, Ermanno Bosgoed, Dorien Lugtenberg, Su Ming Sun, Jordi Corominas Galbany, Marjan Weiss, Marinus J. Blok, Richelle A. C. M. Olde Keizer, Tom Hofste, Debby Hellebrekers, Nicole de Leeuw, Alexander Stegmann, Erik-Jan Kamsteeg, Aimee D. C. Paulussen, Marjolijn J. L. Ligtenberg, Xiangqun Zheng Bradley, John Peden, Alejandra Gutierrez, Adam Pullen, Tom Payne, Christian Gilissen, Arthur van den Wijngaard, Han G. Brunner, Marcel Nelen, Helger G. Yntema, Lisenka E. L. M. Vissers

    Diterbitkan 2024-02-01
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  7. 7
    Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing

    Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing oleh Anouk E. J. Janssen, Rebekka M. Koeck, Rick Essers, Ping Cao, Wanwisa van Dijk, Marion Drüsedau, Jeroen Meekels, Burcu Yaldiz, Maartje van de Vorst, Bart de Koning, Debby M. E. I. Hellebrekers, Servi J. C. Stevens, Su Ming Sun, Malou Heijligers, Sonja A. de Munnik, Chris M. J. van Uum, Jelle Achten, Lars Hamers, Marjan Naghdi, Lisenka E. L. M. Vissers, Ron J. T. van Golde, Guido de Wert, Jos C. F. M. Dreesen, Christine de Die-Smulders, Edith Coonen, Han G. Brunner, Arthur van den Wijngaard, Aimee D. C. Paulussen, Masoud Zamani Esteki

    Diterbitkan 2024-09-01
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