Hasil Pencarian - Erik Boot

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  1. 1
    The ‘End’ of the Maya Long Count? 2012 and the Classic Maya

    The ‘End’ of the Maya Long Count? 2012 and the Classic Maya oleh Erik Boot

    Diterbitkan 2013-06-01
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  2. 2
    P112: Updated clinical practice guidelines for managing children and adults with 22q11.2 deletion syndrome*

    P112: Updated clinical practice guidelines for managing children and adults with 22q11.2 deletion syndrome* oleh Anne Bassett, Solveig Oskarsdottir, Erik Boot, Donna McDonald-McGinn

    Diterbitkan 2023-01-01
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  3. 3
    Correction: Proton Magnetic Resonance Spectroscopy in 22q11 Deletion Syndrome.

    Correction: Proton Magnetic Resonance Spectroscopy in 22q11 Deletion Syndrome. oleh Fabiana da Silva Alves, Erik Boot, Nicole Schmitz, Aart Nederveen, Jacob Vorstman, Christina Lavini, Petra Pouwels, Lieuwe de Haan, Don Linszen, Therese van Amelsvoort

    Diterbitkan 2011-01-01
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  4. 4
    Proton magnetic resonance spectroscopy in 22q11 deletion syndrome.

    Proton magnetic resonance spectroscopy in 22q11 deletion syndrome. oleh Fabiana da Silva Alves, Erik Boot, Nicole Schmitz, Aart Nederveen, Jacob Vorstman, Christina Lavini, Petra J Pouwels, Lieuwe de Haan, Don Linszen, Therese van Amelsvoort

    Diterbitkan 2011-01-01
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  5. 5
    Functional gene-expression analysis shows involvement of schizophrenia-relevant pathways in patients with 22q11 deletion syndrome.

    Functional gene-expression analysis shows involvement of schizophrenia-relevant pathways in patients with 22q11 deletion syndrome. oleh Nico J M van Beveren, Lianne C Krab, Sigrid Swagemakers, Gabriëlle H S Buitendijk, Erik Boot, Peter van der Spek, Ype Elgersma, Therese A M J van Amelsvoort

    Diterbitkan 2012-01-01
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  6. 6
    Correction: Functional Gene-Expression Analysis Shows Involvement of Schizophrenia-Relevant Pathways in Patients with 22q11 Deletion Syndrome.

    Correction: Functional Gene-Expression Analysis Shows Involvement of Schizophrenia-Relevant Pathways in Patients with 22q11 Deletion Syndrome. oleh Nico J. M. van Beveren, Lianne C. Krab, Sigrid Swagemakers, Gabriëe H.S. Buitendijk, Erik Boot, Peter van der Spek, Ype Elgersma, Therese A. M. J. van Amelsvoort

    Diterbitkan 2012-01-01
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  7. 7
    22q11.2 microdeletion and increased risk for type 2 diabetes

    22q11.2 microdeletion and increased risk for type 2 diabetes oleh Lily Van, Tracy Heung, Sarah L. Malecki, Christian Fenn, Andrea Tyrer, Marcos Sanches, Eva W.C. Chow, Erik Boot, Maria Corral, Satya Dash, Susan R. George, Anne S. Bassett

    Diterbitkan 2020-09-01
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  8. 8
    Optometry in adults with microdeletion 22q11.2: The eye as a window to the brain

    Optometry in adults with microdeletion 22q11.2: The eye as a window to the brain oleh Emma N.M.M. von Scheibler, Abhishek Appaji, Tos T.J.M. Berendschot, Noël J.C. Bauer, Naren P. Rao, Agnies M. van Eeghen, Thérèse A.M.J. van Amelsvoort, Erik Boot

    Diterbitkan 2023-12-01
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  9. 9
    Do we care? Reporting of genetic diagnoses in multidisciplinary intellectual disability care: a retrospective chart review

    Do we care? Reporting of genetic diagnoses in multidisciplinary intellectual disability care: a retrospective chart review oleh Annelieke R. Müller, Erik Boot, Stijn B. Notermans, Carlo Schuengel, Lidewij Henneman, Martina C. Cornel, Mieke M. van Haelst, Mariëlle Alders, Clara D. M. van Karnebeek, Bas Bijl, Frits A. Wijburg, Agnies M. van Eeghen

    Diterbitkan 2024-09-01
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  10. 10
    Cortical Morphology Differences in Subjects at Increased Vulnerability for Developing a Psychotic Disorder: A Comparison between Subjects with Ultra-High Risk and 22q11.2 Deletion Syndrome.

    Cortical Morphology Differences in Subjects at Increased Vulnerability for Developing a Psychotic Disorder: A Comparison between Subjects with Ultra-High Risk and 22q11.2 Deletion... oleh Geor Bakker, Matthan W A Caan, Wilhelmina A M Vingerhoets, Fabiana da Silva-Alves, Mariken de Koning, Erik Boot, Dorien H Nieman, Lieuwe de Haan, Oswald J Bloemen, Jan Booij, Thérèse A M J van Amelsvoort

    Diterbitkan 2016-01-01
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  11. 11
    Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders

    Rare copy number variations affecting the synaptic gene DMXL2 in neurodevelopmental disorders oleh Gregory Costain, Susan Walker, Bob Argiropoulos, Danielle A. Baribeau, Anne S. Bassett, Erik Boot, Koen Devriendt, Barbara Kellam, Christian R. Marshall, Aparna Prasad, Moises A. Serrano, D. James Stavropoulos, Hope Twede, Joris R. Vermeesch, Jacob A. S. Vorstman, Stephen W. Scherer

    Diterbitkan 2019-02-01
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