Salta al contenuto
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
Lingua
Tutti i Campi
Titolo
Autore
Soggetto
Collocazione
ISBN/ISSN
Tag
Cerca
Avanzata
Homozygous deletion of FMS in...
Citazione
Invia SMS
Invia email
Stampa
Esporta il record
Esporta a RefWorks
Esporta a EndNoteWeb
Esporta a EndNote
PLink permanente
Homozygous deletion of FMS in a patient with the 5q- syndrome.
Dettagli Bibliografici
Autori principali:
Boultwood, J
,
Rack, K
,
Buckle, V
,
Kelly, S
,
Madden, J
,
Oscier, D
,
Wainscoat, J
Natura:
Journal article
Lingua:
English
Pubblicazione:
1990
Posseduto
Descrizione
Documenti analoghi
MARC21
Documenti analoghi
Loss of both CSF1R (FMS) alleles in patients with myelodysplasia and a chromosome 5 deletion.
di: Boultwood, J, et al.
Pubblicazione: (1991)
Hematological features of patients with myelodysplastic syndromes associated with a chromosome 5q deletion.
di: Lewis, S, et al.
Pubblicazione: (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
di: Boultwood, J, et al.
Pubblicazione: (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.
di: Boultwood, J, et al.
Pubblicazione: (1994)
Structure of the granulocyte macrophage colony-stimulating factor gene in patients with the myelodysplastic syndromes.
di: Boultwood, J, et al.
Pubblicazione: (1990)