J de Grouchy, C Turleau. Show Affiliations »
Abstract
Mesh: See more » Beckwith-Wiedemann Syndrome/geneticsBrain/abnormalitiesChromosome AberrationsCytogeneticsDiGeorge Syndrome/geneticsExostoses, Multiple Hereditary/geneticsEye Neoplasms/geneticsHumansIris/abnormalitiesKaryotypingPrader-Willi Syndrome/geneticsRetinoblastoma/geneticsSyndrome
Year: 1986 PMID: 3533601 DOI: 10.1007/bf01941282
Source DB: PubMed Journal: Experientia ISSN: 0014-4754