Items where authors include "Matthijs, G."

Article

Souche, E., Beltran, S., Brosens, E. et al. (28 more authors) (2022) Recommendations for whole genome sequencing in diagnostics for rare diseases. European Journal of Human Genetics, 30 (9). pp. 1017-1021. ISSN 1018-4813

Foulquier, F., Ungar, D., Reynders, E. et al. (9 more authors) (2007) A new inborn error of glycosylation due to a Cog8 deficiency reveals a critical role for the Cog1-Cog8 interaction in COG complex formation. Human Molecular Genetics, 16 (7). pp. 717-730. ISSN 0964-6906