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Homozygous deletion of FMS in...
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Stalna poveznica
Homozygous deletion of FMS in a patient with the 5q- syndrome.
Bibliografski detalji
Glavni autori:
Boultwood, J
,
Rack, K
,
Buckle, V
,
Kelly, S
,
Madden, J
,
Oscier, D
,
Wainscoat, J
Format:
Journal article
Jezik:
English
Izdano:
1990
Primjerci
Opis
Slični predmeti
Prikaz za djelatnike knjižnice
Slični predmeti
Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.
od: Boultwood, J, i dr.
Izdano: (1991)
Hematological features of patients with myelodysplastic syndromes associated with a chromosome 5q deletion.
od: Lewis, S, i dr.
Izdano: (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
od: Boultwood, J, i dr.
Izdano: (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.
od: Boultwood, J, i dr.
Izdano: (1994)
Structure of the granulocyte macrophage colony-stimulating factor gene in patients with the myelodysplastic syndromes.
od: Boultwood, J, i dr.
Izdano: (1990)