Freire, M. V., MARTIN, M., Thissen, R., Van Marcke, C., SEGERS, K., SEPULCHRE, E., LEROI, N., LETE, C., FASQUELLE, C., Radermacher, J., Gokburun, Y., COLLIGNON, J., Sacré, A., JOSSE, C., PALMEIRA, L., & BOURS, V. (2022). Case Report Series: Aggressive HR Deficient Colorectal Cancers Related to BRCA1 Pathogenic Germline Variants. Frontiers in Oncology, 12, 835581. doi:10.3389/fonc.2022.835581 |
DOCAMPO MARTINEZ, E., MARTIN, M., GANGOLF, M., HARVENGT, J., BULK, S., SEGERS, K., LEROI, N., LETE, C., PALMARICCIOTTI, V., Freire Chadrina, M., LAMBERT, F., & Bours, V. (2021). Hérédité et cancer. Revue Médicale de Liège, 76 (5-6), 327-336. |
Milovidova, T., Schagina, O., Freire Chadrina, M., Demina, N., Filatova, A., Skoblov, M., Stepanova, A., Chuhrova, A., & Polyakov, A. (15 July 2019). X‐linked hypohidrotic ectodermal dysplasia: clinical and molecular genetic analysis of a large Russian family with a synonymous p.Ser267= (c.801A>G) splice site mutation [letter to the editor]. Journal of the European Academy of Dermatology and Venereology, 33 (12), 468-e470. doi:10.1111/jdv.15798 |
Filatova, A., Freire Chadrina, M., Lozier, E., Konovalov, F., Bessonova, L., Iudina, E., Gnetetskaya, V., Kanivets, I., Korostelev, S., & Skoblov, M. (28 November 2018). Novel KIAA1109 variants affecting splicing in a Russian family with ALKURAYA-KUČINSKAS syndrome [letter to the editor]. Clinical Genetics, 95 (3), 440-441. doi:10.1111/cge.13472 |