Response to "Characteristics of 2p15-p16.1 microdeletion syndrome: review and description of two additional patients"

Congenit Anom (Kyoto). 2015 Nov;55(4):191-2. doi: 10.1111/cga.12119.

Authors

Luisa Ronzoni¹, Veronica Saletti², Giulietta Scuvera¹, Susanna Esposito¹, Donatella Milani¹

Affiliations

¹ Pediatric Highly Intensive Care Unit, Department of Pathophysiology and Transplantation, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Università degli Studi di Milano, Milan, Italy.
² Developmental Neurology Unit, Neurological Institute Fondazione IRCCS C.Besta, Milan, Italy.

PMID: 26153024
DOI: 10.1111/cga.12119

No abstract available

Publication types

Letter
Comment

MeSH terms

Abnormalities, Multiple / genetics*
Brain / pathology*
Chromosome Deletion*
Chromosomes, Human, Pair 2 / genetics*
Female
Humans
Male