J L Mandel. Show Affiliations »
Abstract
Mesh: See more » Base SequenceFemaleFragile X Syndrome/geneticsFragile X Syndrome/prevention & controlGenetic TestingHumansHuntington Disease/geneticsHuntington Disease/prevention & controlMaleMuscular Atrophy, Spinal/geneticsMyotonic Dystrophy/geneticsRepetitive Sequences, Nucleic Acid
Year: 1993 PMID: 8513331 DOI: 10.1038/ng0593-8
Source DB: PubMed Journal: Nat Genet ISSN: 1061-4036 Impact factor: 38.330