D Lacombe1. Show Affiliations » 1. Service de génétique médicale, CHU Pellegrin, 33076 Bordeaux, France.
Abstract
Mesh: See more » Abnormalities, Multiple/geneticsChromosome DeletionChromosomes, Human, Pair 22/geneticsCraniofacial Abnormalities/etiologyCraniofacial Abnormalities/geneticsHumansKidney/abnormalitiesLimb Deformities, Congenital/geneticsPhenotype
Year: 2002 PMID: 12108232 DOI: 10.1016/s0929-693x(01)00908-3
Source DB: PubMed Journal: Arch Pediatr ISSN: 0929-693X Impact factor: 1.180