P W Allderdice, W D Heneghan, E T Felismino. Show Affiliations »
Abstract
Entities: Gene
Mesh: See more » Abnormalities, Multiple/geneticsChromosome AberrationsChromosome DeletionChromosomes, Human, 6-12 and XHumansInfant, NewbornKaryotypingMalePedigreeSkull/abnormalitiesSyndrome
Year: 1976 PMID: 953216
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844