Two Modes of Germline Instability at Human Minisatellite MS1 (Locus D1S7): Complex Rearrangements and Paradoxical Hyperdeletion
- 1 June 2003
- journal article
- Published by Elsevier in American Journal of Human Genetics
- Vol. 72 (6) , 1436-1447
- https://doi.org/10.1086/375629
Abstract
No abstract availableKeywords
This publication has 42 references indexed in Scilit:
- Meiotic Recombination and Flanking Marker Exchange at the Highly Unstable Human Minisatellite CEB1 (D2S90)American Journal of Human Genetics, 2000
- Somatic versus Germline Mutation Processes at Minisatellite CEB1 (D2S90) in Humans and Transgenic MiceGenomics, 2000
- Interruptions in the Triplet Repeats of SCA1 and FRAXA Reduce the Propensity and Complexity of Slipped Strand DNA (S-DNA) FormationBiochemistry, 1998
- Full length articleMutation Research - Fundamental and Molecular Mechanisms of Mutagenesis, 1997
- Mutations occurring at the human minisatellite MS1 integrated in haploid yeast are similar to MS1 mutations in humansMolecular Genetics and Genomics, 1997
- Somatic mutation processes at a human minisatelliteHuman Molecular Genetics, 1997
- Mutation rate heterogeneity and the generation of allele diversity at the human minisatellite MS205 (D16S309)Human Molecular Genetics, 1996
- Somatic mutations in VNTR-Locus D1S7 in human colorectal carcinomas are associated with microsatellite instabilityHuman Mutation, 1995
- Minisatellite mutation rate variation associated with a flanking DNA sequence polymorphismNature Genetics, 1994
- Allelic diversity at minisatellite MS205 (D16S309): evidence for polarized variabilityHuman Molecular Genetics, 1993