A S Teebi. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Chromosomes, Human, Pair 22Fetal Growth Retardation/geneticsGene DeletionHumansHypoparathyroidism/geneticsMicrocephaly/geneticsPhenotypePsychomotor Disorders/geneticsSyndromeTerminology as Topic
Year: 2000 PMID: 10712106 PMCID: PMC1734523 DOI: 10.1136/jmg.37.2.145
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318