Detection of Chromosomal Aberrations by a Whole-Genome Microsatellite Screen

This publication has 18 references indexed in Scilit:

• Characterization of familial partial 10p trisomy by chromosomal microdissection, FISH, and microsatellite dosage analysis
  Human Genetics, 1996
• Multicolor Spectral Karyotyping of Human Chromosomes
  Science, 1996
• Karyotyping human chromosomes by combinatorial multi-fluor FISH
  Nature Genetics, 1996
• Detection of a subtle rearrangement of chromosome 22 using molecular techniques
  American Journal of Medical Genetics, 1995
• Uniparental disomy in humans: development of an imprinting map and its implications for prenatal diagnosis
  Human Molecular Genetics, 1995
• The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation
  Nature Genetics, 1995
• Detection of cryptic chromosomal abnormalities in unexplained mental retardation: a general strategy using hypervariable subtelomeric DNA polymorphisms.
  1993
• Mutation of human short tandem repeats
  Human Molecular Genetics, 1993
• Interstitial and terminal deletions of the long arm of chromosome 4: Further delineation of phenotypes
  American Journal of Medical Genetics, 1988
• Incomplete trisomy 22
  Human Genetics, 1981