B Dutrillaux, C Laurent, J M Robert, J Lejeune. Show Affiliations »
Abstract
Mesh: See more » Abnormalities, Multiple/geneticsAdultAneuploidyChromosome Aberrations/geneticsChromosome DisordersChromosomes, Human, 6-12 and XCraniofacial Dysostosis/geneticsCrossing Over, GeneticEyelids/abnormalitiesFemaleGenotypeHumansInfantInfant, NewbornKaryotypingMaleMicrophthalmos/geneticsPhenotypeRecombination, Genetic
Year: 1973 PMID: 4752866 DOI: 10.1159/000130460
Source DB: PubMed Journal: Cytogenet Cell Genet ISSN: 0301-0171