Researcher
Femke Hannes
- Disciplines:Genetics, Systems biology, Molecular and cell biology
Affiliations
- Laboratory for Cytogenetics and Genome Research (Division)
Member
From1 Apr 2009 → 24 Jun 2015
Publications
1 - 10 of 15
- A microdeletion proximal of the critical deletion region is associated with mild Wolf-Hirschhorn syndrome(2012)
Authors: Femke Hannes, Peter Hammond, Oliver Quarrell, Jean-Pierre Fryns, Koenraad Devriendt, Joris Vermeesch
Pages: 996 - 1004 - Characterising the functional consequences of haploinsufficiency of NELF-A (WHSC2) and SLBP identifies novel cellular phenotypes in Wolf-Hirshhorn syndrome(2012)
Authors: Femke Hannes, Joris Vermeesch
Pages: 2181 - 2193 - A microdeletion proximal of the critical deletion region is associated with mild Wolf-Hirschhorn syndrome(2012)
Authors: Femke Hannes, Peter Hammond, Jean-Pierre Frijns, Koenraad Devriendt, Joris Vermeesch
Pages: 996 - 1004 - Fine-grained facial phenotype-genotype analysis in Wolf-Hirschhorn syndrome(2012)
Authors: Peter Hammond, Femke Hannes, Koenraad Devriendt, Joris Vermeesch
Pages: 33 - 40 - The Molecular Dissection of Contiguous Gene Syndromes with a Focus on 4p16 Deletion Syndrome(2011)
Authors: Femke Hannes, Joris Vermeesch, Jean-Pierre Frijns
Number of pages: 192 - Telomere healing following DNA polymerase arrest-induced breakages is likely the main mechanism generating chromosome 4p terminal deletions(2010)
Authors: Femke Hannes, Jeroen Van Houdt, Jean-Pierre Frijns, Joris Vermeesch
Pages: 1343 - 1351 - Duplication of the Wolf-Hirschhorn syndrome critical region causes neurodevelopmental delay(2010)
Authors: Femke Hannes, Joris Vermeesch
Pages: 136 - 140 - Recurrent reciprocal deletions and duplications of 16p13.11: the deletion is a risk factor for MR/MCA while the duplication may be a rare benign variant(2009)
Authors: Femke Hannes, Thomy de Ravel de l'Argentière, Jean-Pierre Frijns, Koenraad Devriendt, Griet Van Buggenhout, Annick Vogels, Joris Vermeesch
Pages: 223 - 232 - An experimental loop design improves the detection of congenital chromosomal aberrati(2009)
Authors: Joke Allemeersch, Steven Van Vooren, Femke Hannes, Bart De Moor, Joris Vermeesch, Yves Moreau
- An experimental loop design improves the detection of congenital chromosomal aberrati(2009)
Authors: Steven Van Vooren, Femke Hannes, Bart De Moor, Joris Vermeesch, Yves Moreau
Patents
1 - 2 of 2