Bénédicte Demeer
5PUBLICATIONS
14CO-AUTHORS
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Publications (5)
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|Aug 14, 2023
Low risk of embryonic and other cancers in PIK3CA-related overgrowth spectrum: Impact on screening recommendations.Laurence Faivre, Jean-Charles Crépin, Manon Réda
|Oct 27, 2019
Likely Pathogenic Variants in One Third of Non-Syndromic Discontinuous Cleft Lip and Palate Patients.Bénédicte Demeer, Nicole Revencu, Raphael Helaers
|Mar 30, 2019
Whole genome paired-end sequencing elucidates functional and phenotypic consequences of balanced chromosomal rearrangement in patients with developmental disorders.Caroline Schluth-Bolard, Flavie Diguet, Nicolas Chatron
|Jan 12, 2019
Fetal phenotype of Rubinstein-Taybi syndrome caused by CREBBP mutations.Julien Van-Gils, Sophie Naudion, Jérôme Toutain
|Nov 22, 2018
Unmasking familial CPX by WES and identification of novel clinical signs.Bénédicte Demeer, Nicole Revencu, Raphael Helaers
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Frequent Collaborators
1 joint publications
Julien Van-Gils
1 joint publications
Caroline Schluth-Bolard
1 joint publications
Patrick Callier
1 joint publications
Raphael Helaers
1 joint publications
Stéphanie Dakpe
1 joint publications
Manon Réda
1 joint publications
Sophie Nambot
1 joint publications
Tristan Mirault
1 joint publications
Nicolas Chassaing
1 joint publications
Salima El Chehadeh
