P Girardet, L Grosset, E Juillard. Show Affiliations »
Abstract
Mesh： See more » Abnormalities, MultipleAlopecia Areata/geneticsChild, PreschoolChromosomes, Human, 16-18Chromosomes, Human, 21-22 and YCytogeneticsDown Syndrome/geneticsFemaleHepatitis/congenitalHumansInfantKaryotypingMaternal AgeMosaicismSkull/abnormalitiesSyndromeTrisomy
Year: 1972 PMID： 4265243
Source DB: PubMed Journal: Helv Paediatr Acta ISSN： 0018-022X