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Publications by E. Lapi

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

Neurogenetics
Molecular NeuroscienceGeneticsCellular
2018English

13q Deletion and Central Nervous System Anomalies: Further Insights From Karyotype-Phenotype Analyses of 14 Patients

Journal of Medical Genetics
Genetics
2006English

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