Emanuele Agolini

发表

Integration of Cytochrome P450 2D6 (CYP2D6) Gene-Drug Results into a Clinical Decision Support System

Mark J. Ratain, Kiang-Teck J. Yeo, Samuel L. Volchenboum, 2016, CRI.

Helsmoortel-Van der Aa Syndrome as emerging clinical diagnosis in intellectually disabled children with autistic traits and ocular involvement.

Antonio Novelli, Emanuele Agolini, Maria Cristina Digilio, 2018, European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society.

Primary muscle involvement in a 15‐year‐old girl with the recurrent homozygous c.362dupC variant in FKBP14

Antonio Novelli, Giuseppe Guglielmi, Enrico Bertini, 2019, American journal of medical genetics. Part A.

Mutations in ANKRD11 cause KBG syndrome, characterized by intellectual disability, skeletal malformations, and macrodontia.

Mustafa Tekin, Bruno Dallapiccola, Juan I. Young, 2011, American journal of human genetics.