H Saraux. Show Affiliations »
Abstract
Mesh: See more » Chromosome Aberrations/complicationsChromosome DisordersChromosomes, Human, 13-15Chromosomes, Human, 16-18Chromosomes, Human, 21-22 and YChromosomes, Human, 6-12 and XCri-du-Chat SyndromeDown SyndromeEye ManifestationsFemaleHumansKaryotypingMaleOptic AtrophyRetinal Degeneration/complicationsRetinitis PigmentosaTrisomy
Year: 1970 PMID: 4249879 PMCID: PMC1468888 DOI: 10.1136/jmg.7.3.227
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318