Sex–dependent rearrangements resulting in CMT1A and HNPP

This publication has 13 references indexed in Scilit:

• A de Novo Case of Hereditary Neuropathy with Liability to Pressure Palsies (HNPP) of Maternal Origin: A New Mechanism for Deletion in 17p11.2?
  Human Molecular Genetics, 1996
• Analysis of the CMT1A-REP repeat: mapping crossover breakpoints in CMT1A and HNPP
  Human Molecular Genetics, 1995
• Two autosomal dominant neuropathies result from reciprocal DNA duplication/deletion of a region on chromosome 17
  Human Molecular Genetics, 1994
• Detection of deletion within 17p11.2 in 7 French families with hereditary neuropathy with liability to pressure palsies (HNPP)
  Cytogenetic and Genome Research, 1994
• Origin of the de novo duplication in Charcot — Marie — Tooth disease type 1A: unequal nonsister chromatid exchange during spermatogenesis
  Human Molecular Genetics, 1993
• DNA deletion associated with hereditary neuropathy with liability to pressure palsies
  Cell, 1993
• Charcot–Marie–Tooth type 1A duplication appears to arise from recombination at repeat sequences flanking the 1.5 Mb monomer unit
  Nature Genetics, 1992
• DNA duplication associated with Charcot-Marie-Tooth disease type 1A
  Cell, 1991
• Duplication in chromosome 17p11.2 in Charcot-Marie-Tooth neuropathy type 1a (CMT 1a)
  Neuromuscular Disorders, 1991
• A partial deletion of the muscular dystrophy gene transmitted twice by an unaffected male
  Nature, 1987