K Wrogemann1, V Biancalana, D Devys, G Imbert, Y Trottier, J L Mandel. Show Affiliations » 1. LGME/CNRS, Institut de Chimie Biologique, Faculté de Médecine, Strasbourg, France.
Abstract
Entities: Disease
Mesh: See more » Base SequenceDNA FingerprintingDNA Mutational AnalysisDNA, Satellite/geneticsFemaleFragile X Syndrome/geneticsGenetic Diseases, Inborn/geneticsHumansMaleMuscular Atrophy, Spinal/geneticsMyotonic Dystrophy/geneticsOligodeoxyribonucleotides/geneticsRepetitive Sequences, Nucleic Acid
Substances: See more » DNA, SatelliteOligodeoxyribonucleotides
Year: 1993 PMID: 8400686 DOI: 10.1007/978-3-0348-8583-6_13
Source DB: PubMed Journal: EXS ISSN: 1023-294X