C P Chen, S P Linn, C S Ho, S R Chern, C C Lee, W L Chen, W Wang. Show Affiliations »
Abstract
Entities: Disease Species
Mesh: See more » AdultChildChromosome DeletionChromosomes, Human, Pair 3/geneticsEpilepsy/complicationsEpilepsy/geneticsHumansKaryotypingMaleMonosomy/geneticsMothersSyndrome
Year: 2005 PMID: 16440889
Source DB: PubMed Journal: Genet Couns ISSN: 1015-8146