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  1. Vanfleteren, Stephan [Photographer] ; Stevens, Ineke [Writer of added text]; Heylen, Martin [Writer of added text]; Vanfleteren, Stephan [Writer of added text] Galeries Vénitiennes Ostende

    Onze IJslandvissers

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    Lichtervelde: Hannibal, [2021]

  2. Lelieveld, Stefan H; Reijnders, Margot R F; Pfundt, Rolph; Yntema, Helger G; Kamsteeg, Erik-Jan; de Vries, Petra; de Vries, Bert B A; Willemsen, Marjolein H; Kleefstra, Tjitske; Löhner, Katharina; Vreeburg, Maaike; Stevens, Servi J C; van der Burgt, Ineke; Bongers, Ernie M H F; Stegmann, Alexander P A; Rump, Patrick; Rinne, Tuula; Nelen, Marcel R; Veltman, Joris A; Vissers, Lisenka E L M; Brunner, Han G; Gilissen, Christian

    Meta-analysis of 2,104 trios provides support for 10 new genes for intellectual disability

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    Springer Science and Business Media LLC, 2016

    Published in: Nature Neuroscience

  3. Stessman, Holly A.F.; Willemsen, Marjolein H.; Fenckova, Michaela; Penn, Osnat; Hoischen, Alexander; Xiong, Bo; Wang, Tianyun; Hoekzema, Kendra; Vives, Laura; Vogel, Ida; Brunner, Han G.; van der Burgt, Ineke; Ockeloen, Charlotte W.; Schuurs-Hoeijmakers, Janneke H.; Klein Wassink-Ruiter, Jolien S.; Stumpel, Connie; Stevens, Servi J.C.; Vles, Hans S.; Marcelis, Carlo M.; van Bokhoven, Hans; Cantagrel, Vincent; Colleaux, Laurence; Nicouleau, Michael; Lyonnet, Stanislas; [...]

    Disruption of POGZ Is Associated with Intellectual Disability and Autism Spectrum Disorders

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    Elsevier BV, 2016

    Published in: The American Journal of Human Genetics

  4. Redin, Claire; Brand, Harrison; Collins, Ryan L; Kammin, Tammy; Mitchell, Elyse; Hodge, Jennelle C; Hanscom, Carrie; Pillalamarri, Vamsee; Seabra, Catarina M; Abbott, Mary-Alice; Abdul-Rahman, Omar A; Aberg, Erika; Adley, Rhett; Alcaraz-Estrada, Sofia L; Alkuraya, Fowzan S; An, Yu; Anderson, Mary-Anne; Antolik, Caroline; Anyane-Yeboa, Kwame; Atkin, Joan F; Bartell, Tina; Bernstein, Jonathan A; Beyer, Elizabeth; Blumenthal, Ian; [...]

    The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies

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    Springer Science and Business Media LLC, 2017

    Published in: Nature Genetics