T Martin-Denavit, M Till, H Plauchu. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsBrain/pathologyChromosomes, Human, Pair 18Chromosomes, Human, Pair 8Craniofacial Abnormalities/geneticsCytogeneticsFaciesFemaleFetal Growth RetardationHumansIn Situ Hybridization, FluorescenceInfantKaryotypingMalePregnancySyndromeTranslocation, Genetic
Year: 2004 PMID: 15214022 DOI: 10.1002/ajmg.a.30043
Source DB: PubMed Journal: Am J Med Genet A ISSN: 1552-4825 Impact factor: 2.802