Amélie Piton
Institut de Génétique et de Biologie Moléculaire et Cellulaire
14 papers found
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Molecular consequences of PQBP1 deficiency, involved in the X-linked Renpenning syndrome
UploadThe neurodevelopmental and facial phenotype in individuals with a TRIP12 variant
UploadKleefstra syndrome: Recurrence in siblings due to a paternal mosaic mutation
Download from onlinelibrary.wiley.comNovel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment
Download from onlinelibrary.wiley.comSex-specific impact of prenatal androgens on social brain default mode subsystems
Download from doi.orgMutations in DCC cause isolated agenesis of the corpus callosum with incomplete penetrance
Download from www.nature.comMissing publications? Search for publications with a matching author name.