Søgeresultater - Koenraad Devriendt

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  1. 1
    To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts

    To tell or not to tell? A systematic review of ethical reflections on incidental findings arising in genetics contexts af Gabrielle Christenhusz, Koenraad Devriendt, Kris Dierickx

    Udgivet 2012
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  2. 2
    Genetic counseling for susceptibility loci and neurodevelopmental disorders: The del15q11.2 as an example

    Genetic counseling for susceptibility loci and neurodevelopmental disorders: The del15q11.2 as an example af Veerle De Wolf, Nathalie Brison, Koenraad Devriendt, Hilde Peeters

    Udgivet 2013
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  3. 3
    Deletion of Thyroid Transcription Factor-1 Gene in an Infant with Neonatal Thyroid Dysfunction and Respiratory Failure

    Deletion of Thyroid Transcription Factor-1 Gene in an Infant with Neonatal Thyroid Dysfunction and Respiratory Failure af Koenraad Devriendt, Christine Vanhole, Gert Matthijs, Francis de Zegher

    Udgivet 1998
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  4. 4
    Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine Kinase

    Congenital Hereditary Lymphedema Caused by a Mutation That Inactivates VEGFR3 Tyrosine Kinase af Alexandre Irrthum, Marika J. Karkkainen, Koenraad Devriendt, Kari Alitalo, Miikka Vikkula

    Udgivet 2000
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  5. 5
    The annual incidence of DiGeorge/velocardiofacial syndrome.

    The annual incidence of DiGeorge/velocardiofacial syndrome. af Koenraad Devriendt, J. P. Fryns, Geert Mortier, M N van Thienen, Kathelijn Keymolen

    Udgivet 1998
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  6. 6
    Elements of morphology: Standard terminology for the lips, mouth, and oral region

    Elements of morphology: Standard terminology for the lips, mouth, and oral region af John C. Carey, M. Michael Cohen, Cynthia J. Curry, Koenraad Devriendt, Lewis B. Holmes, Alain Verloès

    Udgivet 2009
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  7. 7
    Network Analysis of Differential Expression for the Identification of Disease-Causing Genes

    Network Analysis of Differential Expression for the Identification of Disease-Causing Genes af Daniela Nitsch, Léon-Charles Tranchevent, Bernard Thienpont, Lieven Thorrez, Hilde Van Esch, Koenraad Devriendt, Yves Moreau

    Udgivet 2009
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  8. 8
    A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype?

    A novel CSX/NKX2-5 mutation causes autosomal-dominant AV block: are atrial fibrillation and syncopes part of the phenotype? af Ilse Gutierrez-Roelens, Luc De Roy, Caroline Ovaert, Thierry Sluysmans, Koenraad Devriendt, Han G. Brunner, Miikka Vikkula

    Udgivet 2006
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  9. 9
    Minimum prevalence, birth incidence and cause of death for Prader–Willi syndrome in Flanders

    Minimum prevalence, birth incidence and cause of death for Prader–Willi syndrome in Flanders af Annick Vogels, Jenneke van den Ende, Kathelijn Keymolen, Geert Mortier, Koenraad Devriendt, Eric Legius, J P Fryns

    Udgivet 2003
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  10. 10
    Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing

    Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing af Simon Ardui, Valérie Race, Alena Zablotskaya, Matthew S. Hestand, Hilde Van Esch, Koenraad Devriendt, Gert Matthijs, Joris Vermeesch

    Udgivet 2016
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  11. 11
    An unbiased evaluation of gene prioritization tools

    An unbiased evaluation of gene prioritization tools af Daniela Börnigen, Léon-Charles Tranchevent, Francisco Bonachela-Capdevila, Koenraad Devriendt, Bart De Moor, Patrick De Causmaecker, Yves Moreau

    Udgivet 2012
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  12. 12
    Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autism

    Identification and characterization of the TRIP8 and REEP3 genes on chromosome 10q21.3 as novel candidate genes for autism af Dries Castermans, Joris Vermeesch, Jean‐Pierre Fryns, Jean Steyaert, Wim J.M. Van de Ven, John W.M. Creemers, Koenraad Devriendt

    Udgivet 2007
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  13. 13
    Spectrum of Temporal Bone Abnormalities in Patients with Waardenburg Syndrome and<i>SOX10</i>Mutations

    Spectrum of Temporal Bone Abnormalities in Patients with Waardenburg Syndrome and<i>SOX10</i>Mutations af Monique Elmaleh, Clarisse Baumann, N. Noël‐Pétroff, A. Sekkal, V. Couloigner, Koenraad Devriendt, Meredith Wilson, Sandrine Marlin, G. Sebag, Véronique Pingault

    Udgivet 2012
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  14. 14
    GATA-3 in Human T Cell Helper Type 2 Development

    GATA-3 in Human T Cell Helper Type 2 Development af Alla Skapenko, Jan Leipe, Uwe Niesner, Koenraad Devriendt, Rolf Beetz, Andreas Radbruch, Joachim R. Kalden, Peter E. Lipsky, Hendrik Schulze‐Koops

    Udgivet 2004
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  15. 15
    Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of<i>XLMR</i>genes

    Detection of genomic copy number changes in patients with idiopathic mental retardation by high-resolution X-array-CGH: important role for increased gene dosage of<i>XLMR</i>genes af Guy Froyen, Hilde Van Esch, Marijke Bauters, Karen Hollanders, Suzanna G.M. Frints, Joris Vermeesch, Koenraad Devriendt, Jean‐Pierre Fryns, Peter Marynen

    Udgivet 2007
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  16. 16
    Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1mutation

    Platelet characteristics in patients with X-linked macrothrombocytopenia because of a novel GATA1mutation af Kathleen Freson, Koenraad Devriendt, Gert Matthijs, Achiel Van Hoof, Rita De Vos, Chantal Thys, Kristien Minner, Marc Hoylaerts, Jos Vermylen, Chris Van Geet

    Udgivet 2001
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  17. 17
    Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis

    Deletion of VCX-A due to NAHR plays a major role in the occurrence of mental retardation in patients with X-linked ichthyosis af Hilde Van Esch, Karen Hollanders, Liesbeth Badisco, Cindy Melotte, Paul Van Hummelen, Joris Vermeesch, Koenraad Devriendt, Jean‐Pierre Fryns, Peter Marynen, Guy Froyen

    Udgivet 2005
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  18. 18
    Mutations in the Transcription Factor Gene SOX18 Underlie Recessive and Dominant Forms of Hypotrichosis-Lymphedema-Telangiectasia

    Mutations in the Transcription Factor Gene SOX18 Underlie Recessive and Dominant Forms of Hypotrichosis-Lymphedema-Telangiectasia af Alexandre Irrthum, Koenraad Devriendt, David Chitayat, Gert Matthijs, Conrad P. Glade, Peter M. Steijlen, Jean‐Pierre Fryns, Maurice A. M. Van Steensel, Miikka Vikkula

    Udgivet 2003
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  19. 19
    Neuropsychopathology in 7 Patients with the 22q13 Deletion Syndrome: Presence of Bipolar Disorder and Progressive Loss of Skills

    Neuropsychopathology in 7 Patients with the 22q13 Deletion Syndrome: Presence of Bipolar Disorder and Progressive Loss of Skills af A Denayer, Hilde Van Esch, Thomy de Ravel, Jean‐Pierre Frijns, Griet Van Buggenhout, Annick Vogels, Koenraad Devriendt, J. Geutjens, Paul Thiry, Ann Swillen

    Udgivet 2012
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  20. 20
    Clinical evaluation of long-read sequencing-based episignature detection in developmental disorders

    Clinical evaluation of long-read sequencing-based episignature detection in developmental disorders af Mathilde Geysens, Benjamin Huremagic, Erika Souche, Jeroen Breckpot, Koenraad Devriendt, Hilde Peeters, Griet Van Buggenhout, Hilde Van Esch, Kris Van Den Bogaert, Joris Vermeesch

    Udgivet 2025
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