R P Singh, N T Jaco, V Vigna. Show Affiliations »
Abstract
Entities: Species
Mesh: See more » Chromosome AberrationsChromosome DisordersChromosomes, Human, 1-3HumansInfant, NewbornKaryotypingMalePedigreePierre Robin Syndrome/genetics
Year: 1970 PMID: 5481910 DOI: 10.1001/archpedi.1970.02100110108016
Source DB: PubMed Journal: Am J Dis Child ISSN: 0002-922X