< Terug naar vorige pagina
Publicatie
Leveraging consanguinity in inherited retinal diseases uncovers missing genetic variation : rare novel disease genes and a multitude of novel variants in known disease genes
Boekbijdrage - Boekabstract Conferentiebijdrage
Boek: Belgian Society for Human Genetics, 18th Annual meeting, Abstracts
Aantal pagina's: 1
Jaar van publicatie:2018