Homozygous deletion of FMS in a patient with the 5q- syndrome.
Váldodahkkit: | Boultwood, J, Rack, K, Buckle, V, Kelly, S, Madden, J, Oscier, D, Wainscoat, J |
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Materiálatiipa: | Journal article |
Giella: | English |
Almmustuhtton: |
1990
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Geahča maid
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Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.
Dahkki: Boultwood, J, et al.
Almmustuhtton: (1991) -
Hematological features of patients with myelodysplastic syndromes associated with a chromosome 5q deletion.
Dahkki: Lewis, S, et al.
Almmustuhtton: (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
Dahkki: Boultwood, J, et al.
Almmustuhtton: (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.
Dahkki: Boultwood, J, et al.
Almmustuhtton: (1994) -
Structure of the granulocyte macrophage colony-stimulating factor gene in patients with the myelodysplastic syndromes.
Dahkki: Boultwood, J, et al.
Almmustuhtton: (1990)