Myriam Bronner

Publication Activity (10 Years)

Years Active: 2022-2022
Publications (10 Years): 1

Top Topics

End Stage Renal Disease

Intellectual Disability

Transcription Factor

Ejection Fraction

Top Venues

This page only lists publications with an associated author ORCID identifier.

Publications

Juliette Coursimault, Anne Rovelet-Lecrux, Kévin Cassinari, Elise Brischoux-Boucher, Pascale Saugier-Veber, Alice Goldenberg, Francois Lecoquierre, Nathalie Drouot, Anne-Claire Richard, Gabriella Vera, Sophie Coutant, Olivier Quenez, Marion Rolain, Céline Bonnet, Myriam Bronner, Magalie Lecourtois, Gaël Nicolas
uORF-introducing variants in the 5'UTR of the NIPBL gene as a cause of Cornelia de Lange syndrome. Human mutation 43 (9) (2022)