M Feingold, R S Schwartz. Show Affiliations »
Abstract
Mesh: See more » Agammaglobulinemia/geneticsChildChromosome AberrationsChromosomes, Human, 16-18Cri-du-Chat Syndrome/complicationsHumansMosaicismTrisomy
Year: 1968 PMID: 4176894 DOI: 10.1016/s0140-6736(68)91566-3
Source DB: PubMed Journal: Lancet ISSN: 0140-6736 Impact factor: 79.321