E Pergament, G C Pietra, T Kadotani, H Sato, S Berlow. Show Affiliations »
Abstract
Entities: Disease Species
Mesh: See more » Abnormalities, MultipleChromosome AberrationsChromosome DisordersChromosomes, Human, 16-18HumansHypoparathyroidism/geneticsInfantInfant, NewbornKaryotypingMalePedigree
Year: 1970 PMID: 5440360 DOI: 10.1016/s0022-3476(70)80295-5
Source DB: PubMed Journal: J Pediatr ISSN: 0022-3476 Impact factor: 4.406