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Abstract
Entities: Species
Mesh: See more » Child, PreschoolChromosome AberrationsChromosomes, Human, 19-20Chromosomes, Human, 4-5Cri-du-Chat Syndrome/geneticsHumansKaryotypingMalePedigreePhenotypeTranslocation, Genetic
Year: 1974 PMID: 4462641
Source DB: PubMed Journal: Birth Defects Orig Artic Ser ISSN: 0547-6844