J K Morris. Show Affiliations »
Abstract
Mesh: See more » Chromosomes, Human, XFemaleFragile X Syndrome/diagnosisFragile X Syndrome/geneticsGenes, DominantGenetic Diseases, Inborn/diagnosisGenetic Diseases, Inborn/geneticsGenetic LinkageHumansMaleMass Screening/methodsPrenatal Diagnosis
Year: 2004 PMID: 15153318 DOI: 10.1258/096914104774061010
Source DB: PubMed Journal: J Med Screen ISSN: 0969-1413 Impact factor: 2.136