Amélie Piton
Institut de Génétique et de Biologie Moléculaire et Cellulaire
11 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
UploadDe novo variants in CNOT3 cause a variable neurodevelopmental disorder
UploadSex-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
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