Screening of BRCA1/2 genes mutations and copy number variations in patients with high risk for hereditary breast and ovarian cancer syndrome (HBOC)

por El Ansari, Fatima Zahra, Jouali, Farah, Marchoudi, Nabila, Bennani, Mohcine Mechita, Ghailani, Naima Nourouti, Barakat, Amina, Fekkak, Jamal
Publicado 2020