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