A Detailed Physical and Transcriptional Map of the Region of Chromosome 20 That Is Deleted in Myeloproliferative Disorders and Refinement of the Common Deleted Region

This publication has 74 references indexed in Scilit:

• 14-3-3 and its possible role in co-ordinating multiple signalling pathways
  Trends in Cell Biology, 1996
• The humanCD40gene lies within chromosome 20q deletions associated with myeloid malignancies
  British Journal of Haematology, 1996
• Molecular analysis of chromosome 20q deletions associated with myeloproliferative disorders and myelodysplastic syndromes
  Blood, 1994
• The isochore organization of the human genome and its evolutionary history — a review
  Gene, 1993
• Murine chromosomal location of four hepatocyte-enriched transcription factors: HNf-3α, HNF-3β, HNF-3γ, and HNF-4
  Genomics, 1992
• The development and application of automated gridding for efficient screening of yeast and bacterial ordered libraries
  Genomics, 1992
• Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.
  Proceedings of the National Academy of Sciences, 1991
• Basic local alignment search tool
  Journal of Molecular Biology, 1990
• A 3.5 genome equivalent multi access YAC library: construction, characterisation, screening and storage
  Nucleic Acids Research, 1990
• THE ISOCHORE ORGANIZATION OF THE HUMAN GENOME
  Annual Review of Genetics, 1989