P M Fernhoff. Show Affiliations »
Abstract
Mesh: See more » Abnormalities, Multiple/diagnosisAbnormalities, Multiple/epidemiologyAbnormalities, Multiple/geneticsAdultChildChromosome DeletionChromosomes, Human, Pair 22DiGeorge Syndrome/diagnosisDiGeorge Syndrome/epidemiologyDiGeorge Syndrome/geneticsHumansInfantPhenotypeSyndrome
Year: 2000 PMID: 10931401 DOI: 10.1067/mpd.2000.109024
Source DB: PubMed Journal: J Pediatr ISSN: 0022-3476 Impact factor: 4.406