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Prenatal Diagnosis by Trio Exome Sequencing in Fetuses with Ultrasound Anomalies: A Powerful Diagnostic Tool

Frederic Tran Mau-Them,Julian Delanne,Anne-Sophie Denomme-Pichon,Hana Safraou,Ange-Line Bruel,Antonio Vitobello,Aurore Garde,Sophie Nambot,Nicolas Bourgon,Caroline Racine,Arthur Sorlin,Sebastien Moutton,Nathalie Marle,Thierry Rousseau,Paul Sagot,Emmanuel Simon,Catherine Vincent-Delorme,Odile Boute,Cindy Colson,Florence Petit,Marine Legendre,Sophie Naudion,Caroline Rooryck,Clement Prouteau,Estelle Colin,Agnes Guichet,Alban Ziegler,Dominique Bonneau,Godelieve Morel,Melanie Fradin,Alinoe Lavillaureix,Chloe Quelin,Laurent Pasquier,Sylvie Odent,Gabriella Vera,Alice Goldenberg,Anne-Marie Guerrot,Anne-Claire Brehin,Audrey Putoux,Jocelyne Attia,Carine Abel,Patricia Blanchet,Constance F. Wells, Caroline Deiller,Mathilde Nizon,Sandra Mercier,Marie Vincent,Bertrand Isidor,Jeanne Amiel,Rodolphe Dard,Manon Godin,Nicolas Gruchy,Mederic Jeanne,Elise Schaeffer,Pierre-Yves Maillard,Frederique Payet,Marie-Line Jacquemont,Christine Francannet,Sabine Sigaudy, Marine Bergot,Emilie Tisserant,Marie-Laure Ascencio,Christine Binquet,Yannis Duffourd,Christophe Philippe,Laurence Faivre,Christel Thauvin-Robinet

Frontiers in genetics（2023）

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Key words
exome sequencing (ES),chromosomal microarray,prenatal,fetal,diagnostic yield
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