Searching journal content for Koen Devriendt in author.

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  1. Research: Multiple paralogs and recombination mechanisms contribute to the high incidence of 22q11.2 deletion syndrome
    • Lisanne Vervoort,
    • Nicolas Dierckxsens,
    • Marta Sousa Santos,
    • Senne Meynants,
    • Erika Souche,
    • Ruben Cools,
    • Tracy Heung,
    • Koen Devriendt,
    • Hilde Peeters,
    • Donna M. McDonald-McGinn,
    • Ann Swillen,
    • Jeroen Breckpot,
    • Beverly S. Emanuel,
    • Hilde Van Esch,
    • Anne S. Bassett,
    • and Joris R. Vermeesch
    Genome Res. April 2025 35: 786-797; Published in Advance November 13, 2024, doi:10.1101/gr.279331.124
  2. ARTICLE: Genes in a Refined Smith-Magenis Syndrome Critical Deletion Interval on Chromosome 17p11.2 and the Syntenic Region of the Mouse
    • Weimin Bi,
    • Jiong Yan,
    • Paweł Stankiewicz,
    • Sung-Sup Park,
    • Katherina Walz,
    • Cornelius F. Boerkoel,
    • Lorraine Potocki,
    • Lisa G. Shaffer,
    • Koen Devriendt,
    • Małgorzata J.M. Nowaczyk,
    • Ken Inoue,
    • and James R. Lupski
    Genome Res. May 1, 2002 12: 713-728; doi:10.1101/gr.73702
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