Frequency of new copy number variation in humans
- 1 April 2005
- journal article
- other
- Published by Springer Nature in Nature Genetics
- Vol. 37 (4) , 333-334
- https://doi.org/10.1038/ng0405-333
Abstract
No abstract availableThis publication has 12 references indexed in Scilit:
- Shotgun sequence assembly and recent segmental duplications within the human genomeNature, 2004
- Detection of large-scale variation in the human genomeNature Genetics, 2004
- Large-Scale Copy Number Polymorphism in the Human GenomeScience, 2004
- Complex SNP-related sequence variation in segmental genome duplicationsNature Genetics, 2004
- Direct estimates of human per nucleotide mutation rates at 20 loci causing mendelian diseasesHuman Mutation, 2002
- Recent Segmental Duplications in the Human GenomeScience, 2002
- Comprehensive Detection of Genomic Duplications and Deletions in the DMD Gene, by Use of Multiplex Amplifiable Probe HybridizationAmerican Journal of Human Genetics, 2002
- Inversions disrupting the factor VIII gene are a common cause of severe haemophilia ANature Genetics, 1993
- 242 Breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spreadGenomics, 1991
- The rate of spontaneous mutation of a human geneJournal of Genetics, 1935