A Schmidt, E Passarge, E Seemanová, M Macek. Show Affiliations »
Abstract
Mesh: See more » AmniocentesisFemaleFragile X Syndrome/diagnosisFragile X Syndrome/geneticsHumansKaryotypingMalePregnancySex Chromosome Aberrations/diagnosisSex ChromosomesX Chromosome
Year: 1982 PMID: 7169221 DOI: 10.1007/bf00333539
Source DB: PubMed Journal: Hum Genet ISSN: 0340-6717 Impact factor: 4.132