Sandrine Passemard
0000-0002-0242-4566
3 papers found
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De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability
Phenotypes and genotypes in non‐consanguineous and consanguineous primary microcephaly: High incidence of epilepsy
Autosomal recessive primary microcephaly due to ASPM mutations: An update
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