Further delineation of the rare GDACCF (global developmental delay, absent or hypoplastic corpus callosum, dysmorphic facies syndrome): Genotype and phenotype of 22 patients with ZNF148 mutations

Katalin Szakszon, Charles Marques Lourenco, Bert Louis Callewaert, David Geneviève, Flavien Rouxel, Denis Morin, Anne Sophie Denommé-Pichon, Antonio Vitobello, Wesley Patterson, Raymond Louie, Filippo Pinto E Vairo, Eric Klee, Charu Kaiwar, Ralitza H. Gavrilova, Katherine E. Agre, Sebastien Jacquemont, Jizi Khadijé, Jacques Giltay, Koen Van Gassen, Gabriella Mer 'Erica Gerkes, Bregje W. Van Bon, Tuula Rinne, Rolph Pfundt, Han G. Brunner, Oana Caluseriu, Ute Grasshoff, Martin Kehrer, Tobias B. Haack, Melik Malek Khelifa, Anke Katharina Bergmann, Anna Maria Cueto-González, Ariadna Campos Martorell, Shwetha Ramachandrappa, Lindsey B. Sawyer, Pascale Fasel, Dominique Braun, Atallah Isis, Andrea Superti-Furga, Vanda McNiven, David Chitayat, Syed Anas Ahmed, Heiko Brennenstuhl, Eva M.C. Schwaibolf, Gladys Battisti, Benoit Parmentier, Servi J.C. Stevens

Research output: Contribution to journal › Article › peer-review

Fingerprint

Dive into the research topics of 'Further delineation of the rare GDACCF (global developmental delay, absent or hypoplastic corpus callosum, dysmorphic facies syndrome): Genotype and phenotype of 22 patients with ZNF148 mutations'. Together they form a unique fingerprint.

Medicine & Life Sciences