Human Meiotic Recombination Products Revealed by Sequencing a Hotspot for Homologous Strand Exchange in Multiple HNPP Deletion Patients

This publication has 46 references indexed in Scilit:

• The human COX10 gene is disrupted during homologous recombination between the 24 kb proximal and distal CMT1A-REPs
  Human Molecular Genetics, 1997
• Double-strand breaks may initiate the inversion mutation causing the Hunter syndrome
  Human Molecular Genetics, 1997
• Charcot-Marie-Tooth Disease and Related Inherited Neuropathies
  Medicine, 1996
• Analysis of the CMT1A-REP repeat: mapping crossover breakpoints in CMT1A and HNPP
  Human Molecular Genetics, 1995
• MEIOTIC RECOMBINATION HOTSPOTS
  Annual Review of Genetics, 1995
• Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17
  Human Molecular Genetics, 1994
• Repetitive sequences involved in the recombination leading to deletion of exon 5 of the low‐density‐lipoprotein receptor gene in a patient with familial hypercholesterolemia
  European Journal of Biochemistry, 1991
• Frequent deletions of the human X chromosome distal short arm result from recombination between low copy repetitive elements
  Cell, 1990
• A multigene deletion in the human IGH constant region locus involves highly homologous hot spots of recombination
  Genomics, 1989
• Intra-chromosomal gene conversion induced by a DNA double-strand break in Saccharomyces cerevisiae
  Journal of Molecular Biology, 1988