Kallmann Syndrome: Mutations in the Genes Encoding Prokineticin-2 and Prokineticin Receptor-2 – topic of research paper in Biological sciences. Download scholarly article PDF and read for free on CyberLeninka open science hub.
Exposition L'homme couture par Brice Hardelin - Fashion Spider
EDP Sciences - Science Publishing Masterclass in Biomedical sciences in partnership with the Université Paris-Saclay, 26-27 September 2022
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients | European Journal of Human Genetics
Claudie Bosc | Fondation Bettencourt Schueller
LASH MAGAZINE: Samuel Rousseau by Brice Hardelin | Image Amplified
J.-P. Hardelin's research works | Institut Pasteur, Paris and other places
J.-P. Hardelin's research works | Institut Pasteur, Paris and other places