C M Gupta, R D Bhate, V Chandar. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » ChildFemaleGenetic Diseases, Inborn/diagnosisHumansSyndromeXeroderma Pigmentosum/diagnosis
Year: 1988 PMID: 3235151 DOI: 10.1007/bf02727846
Source DB: PubMed Journal: Indian J Pediatr ISSN: 0019-5456 Impact factor: 1.967