Case Report: How whole-genome sequencing-based cell-free DNA prenatal testing can help identify a marker mhromosome

por Kleinfinger, Pascale, Brechard, Marie, Luscan, Armelle, Trost, Detlef, Boughalem, Aicha, Mylene Valduga, Serero DR, Stéphane, Costa, Jean-Marc, Lohmann, Laurence
Publicado 2022

Strategy for Use of Genome-Wide Non-Invasive Prenatal Testing for Rare Autosomal Aneuploidies and Unbalanced Structural Chromosomal Anomalies

por Kleinfinger, Pascale, Lohmann, Laurence, Luscan, Armelle, Trost, Detlef, Bidat, Laurent, Debarge, Véronique, Castaigne, Vanina, Senat, Marie-Victoire, Brechard, Marie-Pierre, Guilbaud, Lucie, Le Guyader, Gwenaël, Satre, Véronique, Laurichesse Delmas, Hélène, Lallaoui, Hakima, Manca-Pellissier, Marie-Christine, Boughalem, Aicha, Valduga, Mylene, Hodeib, Farah, Benachi, Alexandra, Costa, Jean Marc
Publicado 2020