M Tolksdorf, H R Wiedmann, U Goll. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, MultipleChromosome AberrationsChromosome DisordersChromosomes, Human, 13-15HumansInfant, NewbornKaryotypingMale
Year: 1969 PMID: 4186961 DOI: 10.1016/s0140-6736(69)90562-5
Source DB: PubMed Journal: Lancet ISSN: 0140-6736 Impact factor: 79.321