R L Summitt. Show Affiliations »
Abstract
Mesh： See more » Abnormalities, Multiple/geneticsChromosome Aberrations/geneticsChromosome DeletionChromosome DisordersChromosomes, Human, 1-3Chromosomes, Human, 13-15Chromosomes, Human, 21-22 and YChromosomes, Human, 4-5Chromosomes, Human, 6-12 and XDown Syndrome/geneticsFemaleHumansInfantIntellectual Disability/geneticsKaryotypingMalePhenotypeTranslocation, GeneticTrisomy
Year: 1978 PMID： 149945
Source DB: PubMed Journal: Pediatr Ann ISSN： 0090-4481 Impact factor: 1.132