Discover open access scientific publications

Search, annotate, share and cite publications

Publications by S. Manouvrier-Hanu

MED13L-related Intellectual Disability: Involvement of Missense Variants and Delineation of the Phenotype

Molecular Neuroscience

English

Unreported RSK2 Missense Mutation in Two Male Sibs With an Unusually Mild Form of Coffin-Lowry Syndrome

Journal of Medical Genetics

English