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Publications by E. Lapi
MED13L-related Intellectual Disability: Involvement of Missense Variants and Delineation of the Phenotype
Neurogenetics
Molecular Neuroscience
Genetics
Cellular
13q Deletion and Central Nervous System Anomalies: Further Insights From Karyotype-Phenotype Analyses of 14 Patients
Journal of Medical Genetics
Genetics