F Rousseau1, D Heitz, J L Mandel. Show Affiliations » 1. INSERM-U. 184/CNRS-LGME, Strasbourg, France.
Abstract
Entities: Disease
Mesh: See more » Base SequenceDNA/geneticsDNA/metabolismFemaleFragile X Syndrome/geneticsHumansMaleMethylationMutationPedigreeRepetitive Sequences, Nucleic AcidX Chromosome
Substances: See more » DNA
Year: 1992 PMID: 1301206 DOI: 10.1002/humu.1380010202
Source DB: PubMed Journal: Hum Mutat ISSN: 1059-7794 Impact factor: 4.878