Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU.
scientific article published on 10 March 2017
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author: Valérie Cormier-Daire, Tania Attié-Bitach, Cédric Le Caignec, Marie Vincent, David J Amor, Carolien G de Kovel, Annick Toutain, Thierry Billette de Villemeur, Rikke S Møller, Sandrine Passemard, Alain Verloes, Delphine Héron, Laurence Faivre, Joris Andrieux, Frenny Sheth, Sandra Chantot-Bastaraud, Mieke van Haelst
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