L Fañanás, C Fuster, R Guillamat, R Miró. Show Affiliations »
Abstract
Entities: Disease Species
Mesh: See more » Chromosome Fragile SitesChromosome FragilityChromosomes, Human, Pair 21HumansKaryotypingSchizophrenia/genetics
Year: 1997 PMID: 9137142 DOI: 10.1176/ajp.154.5.716a
Source DB: PubMed Journal: Am J Psychiatry ISSN: 0002-953X Impact factor: 18.112