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

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

Manylion Llyfryddiaeth
Prif Awduron: Boultwood, J, Rack, K, Buckle, V, Kelly, S, Madden, J, Oscier, D, Wainscoat, J
Fformat: Journal article
Iaith:English
Cyhoeddwyd: 1990
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Eitemau Tebyg

  • Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.
    gan: Boultwood, J, et al.
    Cyhoeddwyd: (1991)
  • Hematological features of patients with myelodysplastic syndromes associated with a chromosome 5q deletion.
    gan: Lewis, S, et al.
    Cyhoeddwyd: (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
    gan: Boultwood, J, et al.
    Cyhoeddwyd: (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.
    gan: Boultwood, J, et al.
    Cyhoeddwyd: (1994)
  • Structure of the granulocyte macrophage colony-stimulating factor gene in patients with the myelodysplastic syndromes.
    gan: Boultwood, J, et al.
    Cyhoeddwyd: (1990)

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