A unique phenotype in a patient with a rare triplication of the 22q11.2 region and new clinical insights of the 22q11.2 microduplication syndrome: a report of two cases
Crossref DOI link: https://doi.org/10.1186/s12887-015-0417-5
Published Online: 2015-08-22
Published Print: 2015-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Vaz, Sara O.
Pires, Renato
Pires, Luís M.
Carreira, Isabel M.
Anjos, Rui
Maciel, Paula
Mota-Vieira, Luisa
License valid from 2015-08-22