P Jalbert, Y Gilbert, P Léopold, C Mouriquand, A Beaudoing. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Cataract/congenitalChromosome Aberrations/complicationsChromosome DisordersChromosomes, Human, 4-5ConsanguinityFemaleHallermann's SyndromeHumansInfant, NewbornKaryotypingMandibulofacial Dysostosis
Year: 1968 PMID: 5739927
Source DB: PubMed Journal: Pediatrie ISSN: 0031-4021