G F Smith, S Sachdeva, N Janakiraman, S N Sinha. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsChromosome Aberrations/geneticsChromosome DisordersChromosomes, Human, 19-20Chromosomes, Human, 21-22 and YFemaleHumansInfant, NewbornKaryotypingMacroglossia/geneticsMicroscopy, FluorescenceSyndromeTongue/abnormalities
Year: 1974 PMID: 4443993 PMCID: PMC1013220 DOI: 10.1136/jmg.11.4.406
Source DB: PubMed Journal: J Med Genet ISSN: 0022-2593 Impact factor: 6.318