T R Cole. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » Beckwith-Wiedemann Syndrome/geneticsChromosomes, Human, Pair 11FemaleGenomic ImprintingGrowth Disorders/complicationsGrowth Disorders/geneticsHumansKidney Neoplasms/geneticsMaleModels, GeneticPhenotypeSyndromeWilms Tumor/geneticsX Chromosome
Year: 1995 PMID: 7710515 PMCID: PMC2033596 DOI: 10.1038/bjc.1995.87
Source DB: PubMed Journal: Br J Cancer ISSN: 0007-0920 Impact factor: 7.640