Human Genomic Deletions Mediated by Recombination between Alu Elements
- 1 July 2006
- journal article
- research article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 79 (1) , 41-53
- https://doi.org/10.1086/504600
Abstract
No abstract availableKeywords
This publication has 61 references indexed in Scilit:
- The Human LINE-1 Retrotransposon Creates DNA Double-strand BreaksJournal of Molecular Biology, 2006
- A high-resolution survey of deletion polymorphism in the human genomeNature Genetics, 2005
- Finishing the euchromatic sequence of the human genomeNature, 2004
- Analysis of the Human Alu Ya-lineageJournal of Molecular Biology, 2004
- Analysis of Primate Genomic Variation Reveals a Repeat-Driven Expansion of the Human GenomeGenome Research, 2003
- Genomewide Comparison of DNA Sequences between Humans and ChimpanzeesAmerican Journal of Human Genetics, 2002
- Alu repeats and human genomic diversityNature Reviews Genetics, 2002
- Initial sequencing and analysis of the human genomeNature, 2001
- AnAlu-mediated 7.1 kb deletion ofBRCA1 exons 8 and 9 in breast and ovarian cancer families that results in alternative splicing of exon 10Genes, Chromosomes and Cancer, 2000
- Unequal homologous recombination between LINE-1 elements as a mutational mechanism in human genetic disease 1 1Edited by J. KarnJournal of Molecular Biology, 1998