Chromosome 17q21.31 duplication syndrome: Description of a new familiar case and further delineation of the clinical spectrum.
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society | 2016-01-01 | PMID 26565673
Natacci Federica, Alfei Enrico, Tararà Lucia and 4 more
