J I Rodríguez, J Palacios, M Urioste, J L Rodríguez-Peralto. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Abnormalities, Multiple/geneticsEctromelia/geneticsGenetic LinkageHumansInfant, NewbornMaleSyndromeX Chromosome
Year: 1992 PMID: 1605264 DOI: 10.1002/ajmg.1320430328
Source DB: PubMed Journal: Am J Med Genet ISSN: 0148-7299