- Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations(2018)
Tijdschrift: Genetics in Medicine : Official Journal of the American College of Medical Genetics
ISSN: 1098-3600
Issue: 2
Volume: 20
Auteurs: Kristof Van Schil, Sarah Naessens, Stijn Van De Sompele, Marjolein Carron, Alexander Aslanidis, Caroline Van Cauwenbergh, Anja Kathrin Mayer, Mattias Van Heetvelde, Miriam Bauwens, Hannah Verdin, et al.
Pagina's: 202 - 213
- Leveraging consanguinity in inherited retinal diseases uncovers missing genetic variation : rare novel disease genes and a multitude of novel variants in known disease genes(2018)
Boek: Belgian Society for Human Genetics, 18th Annual meeting, Abstracts
Auteurs: Kristof Van Schil, Sarah Naessens, Stijn Van De Sompele, Nuria Gruartmoner Roura, Marjolein Carron, Katharina Dannhausen, Sarah De Jaegere, Maxim Vanpanteghem, Frauke Coppieters, Marcus Karlstetter, et al.
Aantal pagina's: 1
- Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations(2017)
Boek: Science Day, Faculty of Medicine and Health Science, Ghent University, Abstracts
Auteurs: Kristof Van Schil, Sarah Naessens, Stijn Van De Sompele, Marjolein Carron, Alexander Aslanidis, Caroline Van Cauwenbergh, Anja Kathrin Mayer, Mattias Van Heetvelde, Miriam Bauwens, Hannah Verdin, et al.
Aantal pagina's: 1
