Cardiovascular Pathology in Males and Females with 45,X/46,XY Mosaicism

Por De Groote, Katya, Cools, Martine, De Schepper, Jean, Craen, Margarita, François, Inge, Devos, Daniel, Carbonez, Karlien, Eyskens, Benedicte, De Wolf, Daniel
Publicado em 2013

Deletion of PREPL, a Gene Encoding a Putative Serine Oligopeptidase, in Patients with Hypotonia-Cystinuria Syndrome

Por Jaeken, Jaak, Martens, Kevin, François, Inge, Eyskens, François, Lecointre, Claudine, Derua, Rita, Meulemans, Sandra, Slootstra, Jerry W., Waelkens, Etienne, Zegher, Francis de, Creemers, John W. M., Matthijs, Gert
Publicado em 2006

Methylation Defect in Imprinted Genes Detected in Patients with an Albright's Hereditary Osteodystrophy Like Phenotype and Platelet Gs Hypofunction

Por Izzi, Benedetta, Francois, Inge, Labarque, Veerle, Thys, Chantal, Wittevrongel, Christine, Devriendt, Koen, Legius, Eric, Van den Bruel, Annick, D'Hooghe, Marc, Lambrechts, Diether, de Zegher, Francis, Van Geet, Chris, Freson, Kathleen
Publicado em 2012

Profiling of conserved non-coding elements upstream of SHOX and functional characterisation of the SHOX cis-regulatory landscape

Por Verdin, Hannah, Fernández-Miñán, Ana, Benito-Sanz, Sara, Janssens, Sandra, Callewaert, Bert, Waele, Kathleen De, Schepper, Jean De, François, Inge, Menten, Björn, Heath, Karen E., Gómez-Skarmeta, José Luis, Baere, Elfride De
Publicado no Sci Rep (2015)

Gain-of-function mutations in signal transducer and activator of transcription 1 (STAT1): Chronic mucocutaneous candidiasis accompanied by enamel defects and delayed dental sheddin...

Por Frans, Glynis, Moens, Leen, Schaballie, Heidi, Van Eyck, Lien, Borgers, Heleen, Wuyts, Margareta, Dillaerts, Doreen, Vermeulen, Edith, Dooley, James, Grimbacher, Bodo, Cant, Andrew, Declerck, Dominique, Peumans, Marleen, Renard, Marleen, De Boeck, Kris, Hoffman, Ilse, François, Inge, Liston, Adrian, Claessens, Frank, Bossuyt, Xavier, Meyts, Isabelle
Publicado no J Allergy Clin Immunol (2014)