Cloning of a Mouse Homologue of the Human Werner Syndrome Gene and Assignment to 8A4 by Fluorescencein SituHybridization
- 15 April 1997
- Vol. 41 (2), 298-300
- https://doi.org/10.1006/geno.1997.4661
Abstract
No abstract availableThis publication has 9 references indexed in Scilit:
- Positional Cloning of the Werner's Syndrome GeneScience, 1996
- Molecular cloning of cDNA encoding human DNA helicase Q1 Which has homology toEscherichia coliRec Q helicase and localization of the gene at chromosome 12p12Nucleic Acids Research, 1994
- Physical and genetic map of 5q31: use of fluorescence in situ hybridization data to identify errors in the CEPH databaseCytogenetic and Genome Research, 1994
- A Physical Map of 15 Loci on Human Chromosome 5q23-q33 by Two-Color Fluorescence in Situ HybridizationGenomics, 1993
- Basic local alignment search toolJournal of Molecular Biology, 1990
- DNA HELICASESAnnual Review of Biochemistry, 1990
- Two related superfamilies of putative helicases involved in replication, recombination, repair and expression of DNA and RNA genomesNucleic Acids Research, 1989
- The recQ gene of Escherichia coli K12: primary structure and evidence for SOS regulationMolecular Genetics and Genomics, 1986
- Family analysis of Werner's syndrome: A survey of 42 Japanese families with a review of the literatureClinical Genetics, 1981