Articles dans des revues avec comité de lecture (3)
1.
Sassi, A., Désir, J., Duerinckx, S., Soblet, J., Van Dooren, S., Bonduelle, M., Abramowicz, M., & Delbaere, A. (2021). Compound heterozygous null mutations of NOBOX in sisters with delayed puberty and primary amenorrhea. Molecular genetics & genomic medicine. doi:10.1002/mgg3.17762.
Sassi, A., Désir, J., Janssens, V., Marangoni, M., Daneels, D., Gheldof, A., Bonduelle, M., Van Dooren, S., Costagliola, S., & Delbaere, A. (2020). Novel inactivating follicle-stimulating hormone receptor mutations in a patient with premature ovarian insufficiency identified by next-generation sequencing gene panel analysis. F and S Reports, 1(3), 193-201. doi:10.1016/j.xfre.2020.08.008