K E Davies. Show Affiliations »
Abstract
Entities: Species
Mesh: See more » FemaleFragile X Syndrome/geneticsGenetic TestingHumansMaleMuscular Atrophy, Spinal/geneticsMutation/geneticsMyotonic Dystrophy/geneticsRepetitive Sequences, Nucleic Acid/genetics
Year: 1992 PMID: 1538769 DOI: 10.1038/356015a0
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962