P S Gerald. Show Affiliations »
Abstract
Mesh: See more » Amino Acid Metabolism, Inborn Errors/geneticsCongenital HypothyroidismFragile X Syndrome/geneticsGalactosemias/geneticsGenetic TestingHumansHypothyroidism/geneticsInfant, NewbornIntellectual Disability/geneticsNew EnglandRegional Medical Programs/organization & administration
Year: 1983 PMID: 6882891
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844