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Displaying 2 results.
    • Journal article
    FOXP1 -related intellectual disability syndrome: a recognisable entity
    Meerschaut, Ilse Rochefort, Daniel Revencu, Nicole[UCL] Pètre, Justine Corsello, Christina Rouleau, Guy A Hamdan, Fadi F Michaud, Jacques L Morton, Jenny Radley, Jessica Ragge, Nicola García-Miñaúr, Sixto Lapunzina, Pablo Bralo, Maria Palomares Mori, Maria Ángeles Moortgat, Stéphanie Benoit, Valérie Mary, Sandrine Bockaert, Nele Oostra, Ann Vanakker, Olivier Velinov, Milen de Ravel, Thomy JL Mekahli, Djalila Sebat, Jonathan Vaux, Keith K DiDonato, Nataliya Hanson-Kahn, Andrea K Hudgins, Louanne Dallapiccola, Bruno Novelli, Antonio Tarani, Luigi Andrieux, Joris Parker, Michael J Neas, Katherine Ceulemans, Berten Schoonjans, An-Sofie Prchalova, Darina Havlovicova, Marketa Hancarova, Miroslava Budisteanu, Magdalena Dheedene, Annelies Menten, Björn Dion, Patrick A Lederer, Damien Callewaert, Bert (2017) Journal of Medical Genetics — Vol. 54, no.9, p. 613-623 (2017)
    • Journal article
    Further delineation of auriculocondylar syndrome based on 14 novel cases and reassessment of 25 published cases.
    Vegas, Nancy Demir, Zeynep Gordon, Christopher T Breton, Sylvain Romanelli Tavares, Vanessa L Moisset, Hugo Zechi-Ceide, Roseli Kokitsu-Nakata, Nancy M Kido, Yasuhiro Marlin, Sandrine Gherbi Halem, Souad Meerschaut, Ilse Callewaert, Bert Chung, Brian Revencu, Nicole[UCL] Lehalle, Daphné Petit, Florence Propst, Evan J Papsin, Blake C Phillips, John H Jakobsen, Linda Le Tanno, Pauline Thévenon, Julien McGaughran, Julie Gerkes, Erica H Leoni, Chiara Kroisel, Peter Tan, Tiong Y Henderson, Alex Terhal, Paulien Basel-Salmon, Lina Alkindy, Adila White, Susan M Passos-Bueno, Maria R Pingault, Véronique De Pontual, Loïc Amiel, Jeanne (2022) Human mutation — Vol. 43, no.5, p. 582-594 (2022)