K S Reddy, I M Thomas, H S Narayanan. Show Affiliations »
Abstract
Mesh: See more » Abnormalities, Multiple/geneticsChromosome DeletionChromosomes, Human, 6-12 and XHumansInfantKaryotypingMaleSyndrome
Year: 1984 PMID: 6511057 DOI: 10.1007/bf02754688
Source DB: PubMed Journal: Indian J Pediatr ISSN: 0019-5456 Impact factor: 1.967