M G Forsythe, H Walker, L Weiss, J R Roberson, M J Worsham, V R Babu, D L Van Dyke. Show Affiliations »
Abstract
Mesh: See more » AdolescentChildChromosome Aberrations/geneticsChromosome DeletionChromosome DisordersChromosomes, Human, Pair 11FemaleFingers/abnormalitiesHumansIntellectual Disability/geneticsKaryotypingMaleMicrognathism/geneticsPedigreePhenotypeTranslocation, Genetic
Year: 1988 PMID: 3250948
Source DB: PubMed Journal: Henry Ford Hosp Med J ISSN: 0018-0416