Skip to content
VuFind
English
Deutsch
Español
Français
Italiano
日本語
Nederlands
Português
Português (Brasil)
中文(简体)
中文(繁體)
Türkçe
עברית
Gaeilge
Cymraeg
Ελληνικά
Català
Euskara
Русский
Čeština
Suomi
Svenska
polski
Dansk
slovenščina
اللغة العربية
বাংলা
Galego
Tiếng Việt
Hrvatski
हिंदी
Հայերէն
Українська
Sámegiella
Монгол
Jezik
Vsa polja
Naslov
Avtor
Tema
Signatura
ISBN/ISSN
Oznaka
Išči
Napredno
Homozygous deletion of FMS in...
Citiraj
Pošljite SMS
Pošljite email
Natisni
Izvozi zadetek
Izvozi v RefWorks
Izvozi v EndNoteWeb
Izvozi v EndNote
Permanent link
Homozygous deletion of FMS in a patient with the 5q- syndrome.
Bibliografske podrobnosti
Main Authors:
Boultwood, J
,
Rack, K
,
Buckle, V
,
Kelly, S
,
Madden, J
,
Oscier, D
,
Wainscoat, J
Format:
Journal article
Jezik:
English
Izdano:
1990
Zaloga
Opis
Podobne knjige/članki
Knjižničarski pogled
Podobne knjige/članki
Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.
od: Boultwood, J, et al.
Izdano: (1991)
Hematological features of patients with myelodysplastic syndromes associated with a chromosome 5q deletion.
od: Lewis, S, et al.
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, et al.
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, et al.
Izdano: (1994)
Structure of the granulocyte macrophage colony-stimulating factor gene in patients with the myelodysplastic syndromes.
od: Boultwood, J, et al.
Izdano: (1990)