R G Weleber, F Hecht, E R Giblett. Show Affiliations »
Abstract
Mesh: See more » Abnormalities, Multiple/geneticsAutoradiographyBlepharoptosis/geneticsChromosome AberrationsChromosome DisordersChromosomes, Human, 21-22 and Y/metabolismDNA ReplicationDermatoglyphicsFemaleHumansInfantIntellectual Disability/geneticsKaryotypingMicrocephaly/geneticsPhenotypeSyndactyly/genetics
Year: 1968 PMID: 4296014 DOI: 10.1001/archpedi.1968.02100010491015
Source DB: PubMed Journal: Am J Dis Child ISSN: 0002-922X