L Roberts. Show Affiliations »
Abstract
Entities: Disease
Mesh: See more » AtrophyChromosome MappingChromosomes, Human, Pair 4Corpus Striatum/pathologyHumansHuntington Disease/geneticsHuntington Disease/pathologyRecombination, Genetic
Year: 1992 PMID: 1439780 DOI: 10.1126/science.1439780
Source DB: PubMed Journal: Science ISSN: 0036-8075 Impact factor: 47.728