J E Gray, J E Syrett, K M Ritchie, W D Elliott. Show Affiliations »
Abstract
Mesh: See more » Cataract/geneticsChild, PreschoolChromosome AberrationsChromosomes, Human, 1-3Chromosomes, Human, 4-5FemaleFollow-Up StudiesHeart Defects, Congenital/geneticsHumansInfantInfant, NewbornIntellectual Disability/geneticsKaryotyping
Year: 1972 PMID: 4113335 DOI: 10.1016/s0140-6736(72)91588-7
Source DB: PubMed Journal: Lancet ISSN: 0140-6736 Impact factor: 79.321