R I Richards1, G R Sutherland. Show Affiliations » 1. Department of Cytogenetics and Molecular Genetics, Adelaide Children's Hospital, Australia.
Abstract
Entities: Species
Mesh: See more » Base SequenceFragile X Syndrome/geneticsGenetic Diseases, Inborn/geneticsHumansMolecular Sequence DataMutationRepetitive Sequences, Nucleic Acid
Year: 1992 PMID: 1516128 DOI: 10.1016/0092-8674(92)90302-s
Source DB: PubMed Journal: Cell ISSN: 0092-8674 Impact factor: 41.582