The Arrival of Exome Sequencing in French Prenatal Diagnosis: An Exploratory Qualitative Study Among Professionals in Prenatal Diagnosis Centers: Prenatome-SHS.

Fiche publication

Date publication

juillet 2025

Journal

Prenatal diagnosis

Auteurs

Membres identifiés du Cancéropôle Est :
Pr BINQUET Christine , Pr FAIVRE Laurence , Pr PHILIPPE Christophe , Dr MEUNIER-BEILLARD Nicolas , Pr THAUVIN-ROBINET Christel

Tous les auteurs :
Daval C, Meunier-Beillard N, Viora-Dupont E, Delanne J, Garde A, Racine C, Mau-Them FT, Denommé-Pichon AS, Philippe C, Bruel AL, Safraou H, Odent S, Quélin C, Legendre M, Naudion S, Jeanne M, Jacquemont ML, Guichet A, Saldana C, Guerrot AM, Goldenberg A, Guégan C, Vincent M, Putoux A, Francannet C, Wells C, Arthuis C, Alexandre E, Rousseau T, Martz O, Simon E, Magnien O, Bobert F, Bert S, Coatleven F, Reveyaz F, Moulinié P, Binquet C, Thauvin-Robinet C, Faivre L

Lien Pubmed

https://www.ncbi.nlm.nih.gov/pubmed/40696537

Résumé

Following the first French multicenter pilot study (AnDDI-Prenatome) focused on the implementation of prenatal exome sequencing (pES), this ancillary study aims to explore the ethical and clinical issues raised by pES within multidisciplinary prenatal diagnosis centers.