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Homozygous deletion of FMS in...
Čujuhandieđut
Deakstadieđáhus
Sádde šleađgaboasttain
Čálit
Doalvvo čujuhusa
Doalvun: RefWorks
Doalvun: EndNoteWeb
Doalvun: EndNote
Bissovaš liŋka
Homozygous deletion of FMS in a patient with the 5q- syndrome.
Bibliográfalaš dieđut
Váldodahkkit:
Boultwood, J
,
Rack, K
,
Buckle, V
,
Kelly, S
,
Madden, J
,
Oscier, D
,
Wainscoat, J
Materiálatiipa:
Journal article
Giella:
English
Almmustuhtton:
1990
Oažžasuvvandieđut
Govvádus
Geahča maid
Bargiidšearbma
Geahča maid
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)