Homozygous deletion of FMS in a patient with the 5q- syndrome.

Títulos similares

• Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.
  por: Boultwood, J, et al.
  Publicado: (1991)
• Hematological features of patients with myelodysplastic syndromes associated with a chromosome 5q deletion.
  por: Lewis, S, et al.
  Publicado: (1995)
• MOLECULAR MAPPING OF UNCHARACTERISTICALLY SMALL 5Q DELETIONS IN 2 PATIENTS WITH THE 5Q- SYNDROME - DELINEATION OF THE CRITICAL REGION ON 5Q AND IDENTIFICATION OF A 5Q- BREAKPOINT
  por: Boultwood, J, et al.
  Publicado: (1993)
• Molecular mapping of uncharacteristically small 5q deletions in two patients with the 5q- syndrome: delineation of the critical region on 5q and identification of a 5q- breakpoint.
  por: Boultwood, J, et al.
  Publicado: (1994)
• Structure of the granulocyte macrophage colony-stimulating factor gene in patients with the myelodysplastic syndromes.
  por: Boultwood, J, et al.
  Publicado: (1990)