Associated Papers
SBIDDS Syndrome: A New Spoke of the Epigenetic Machinery Wheel.
Aleo S et al.
Molecular Syndromology, 2023
Novel PRMT7 mutation in a rare case of dysmorphism and intellectual disability.
Poquérusse J et al.
Journal of Human Genetics, 2022
Further delineation of the phenotype caused by loss of function mutations in PRMT7.
Valenzuela I et al.
European Journal of Medical Genetics, 2019
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