E Bois, P Royer. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AdolescentChildChromosome AberrationsChromosome DisordersConsanguinityFemaleGenes, DominantGenes, RecessiveHeterozygoteHomozygoteHumansKidney Diseases/complicationsKidney Diseases/geneticsKidney TubulesMalePedigreePhenotypeRetinal Degeneration/complicationsRetinal Degeneration/genetics
Year: 1970 PMID: 5425823
Source DB: PubMed Journal: Arch Fr Pediatr ISSN: 0003-9764