P C Mishra, R Singh. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » DermatoglyphicsDwarfism/geneticsHumansHypogonadism/geneticsInfantMaleSyndromeXeroderma Pigmentosum/genetics
Year: 1982 PMID: 7182366 DOI: 10.1007/bf02976985
Source DB: PubMed Journal: Indian J Pediatr ISSN: 0019-5456 Impact factor: 1.967