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Displaying 5 results.
    • Journal article
    Implementation of genomic arrays in prenatal diagnosis: The Belgian approach to meet the challenges
    Vanakker, Olivier Vilain, Catheline Janssens, Katrien Van der Aa, Nathalie Smits, Guillaume Bandelier, Claude[UCL] Blaumeiser, Bettina Bulk, Saskia Caberg, Jean-Hubert De Leener, Anne De Rademaeker, Marjan de Ravel, Thomy Desir, Julie Destree, Anne Dheedene, Annelies Gaillez, Stéphane Grisart, Bernard Hellin, Ann-Cécile Janssens, Sandra Keymolen, Kathelijn Menten, Björn Pichon, Bruno Ravoet, Marie[UCL] Revencu, Nicole[UCL] Rombout, Sonia Staessens, Catherine Van Den Bogaert, Ann Van Den Bogaert, Kris Vermeesch, Joris R. Kooy, Frank Sznajer, Yves[UCL] Devriendt, Koen (2014) European Journal of Medical Genetics — Vol. 57, no. 4, p. 151-156 (2014)
    • Speech
    The Belgian MicroArray Prenatal (BEMAPRE) database [Online Abstract]
    Muys,, J. Janssens, K. Vanakker, O. Vilain, C. Smits, G. Bandelier, Claude[UCL] Bulk, S. Caberg, J. De Leener, A. De Rademaeker, M. de Ravel de l'Argentière, T. Desir, J. Destree, A. Dheedene, A. Gaillez, S. Grisart, B. Hellin, A. Janssens, S. Keymolen, K. Menten, B. Pichon, B. Ravoet, Marie[UCL] Revencu, Nicole[UCL] Rombout, S. Staessens, C. Van Den Bogaert, A. Van Den Bogaert, K. Vermeesch, J. Sznajer, Yves[UCL] Blaumeiser, B. Jacquemyn, Y. Devriendt, K. (2015) European Human Genetics Conference 2015 — (Scotland) Glasgow
    • Journal article
    Tandem inversion duplication within F8 Intron 1 associated with mild haemophilia A.
    Lannoy, Nathalie[UCL] Bandelier, Claude[UCL] Grisart, Bernard Reginster, Michel Ronge-Collard, Elisabeth Vikkula, Miikka[UCL] Hermans, Cédric[UCL] (2015) Haemophilia — Vol. 21, no. 4, p. 516-522 (2015)
    • Journal article
    The Belgian MicroArray Prenatal (BEMAPRE) database: A systematic nationwide repository of fetal genomic aberrations.
    Muys, Joke Blaumeiser, Bettina Jacquemyn, Yves Bandelier, Claude[UCL] Brison, Nathalie Bulk, Saskia Chiarappa, Patrizia[UCL] Courtens, Winnie De Leener, Anne[UCL] De Rademaeker, Marjan Désir, Julie Destrée, Anne Devriendt, Koenraad Dheedene, Annelies Fieuw, Annelies Fransen, Erik Gatot, Jean-Stéphane Holmgren, Philip Jamar, Mauricette Janssens, Sandra Keymolen, Kathelijn Lederer, Damien Menten, Björn Meuwissen, Marije Parmentier, Benoit Pichon, Bruno Rombout, Sonia Sznajer, Yves[UCL] Van Den Bogaert, Ann Van Den Bogaert, Kris Vanakker, Olivier Vermeesch, Joris Janssens, Katrien (2018) Prenatal diagnosis — Vol. 38, no.13, p. 1120-1128 (2018)
    • Journal article
    Severe growth retardation, delayed bone age, and facial dysmorphism in two patients with microduplications in 2p16 → p22
    Blassnig-Ezeh, Anya Bandelier, Claude[UCL] Frühmesser, Anne Revencu, Nicole[UCL] Krabichler, Birgit Beauloye, Véronique[UCL] Ravoet, Marie[UCL] Fauth, Christine Zschocke, Johannes Simma, Burkhard Kotzot, Dieter (2013) American journal of medical genetics. Part A — Vol. 161A, no. 12, p. 3176-3181 (2013)