Grazia M. S. Mancini

A fetus with de novo 2q33.2q35 deletion including MAP2 with brain anomalies, esophageal atresia, and laryngeal stenosis

E. van Binsbergen, N. Canham, J. Jarvis, 2014, American journal of medical genetics. Part A.

Phenotypic variability of atypical 22q11.2 deletions not including TBX1

G. Mancini, P. Willems, L. Hulsman, 2012, American journal of medical genetics. Part A.

Overlapping cortical malformations in patients with pathogenic variants in GRIN1 and GRIN2B

D. Baralle, A. Laquérriere, S. Mansour, 2022, Journal of Medical Genetics.

SYNGAP1 encephalopathy A distinctive generalized developmental and epileptic encephalopathy

I. Scheffer, H. Mefford, S. Berkovic, 2022 .