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Sickle Cell-Hemoglobin D Iran...
Čujuhandieđut
Deakstadieđáhus
Sádde šleađgaboasttain
Čálit
Doalvvo čujuhusa
Doalvun: RefWorks
Doalvun: EndNoteWeb
Doalvun: EndNote
Bissovaš liŋka
Sickle Cell-Hemoglobin D Iran: A Benign Sickle Cell Syndrome
Bibliográfalaš dieđut
Váldodahkkit:
Serjeant, B
,
Myerscough, E
,
Serjeant, G
,
Higgs, D
,
Moo-Penn, W
Materiálatiipa:
Journal article
Almmustuhtton:
1982
Oažžasuvvandieđut
Govvádus
Geahča maid
Bargiidšearbma
Geahča maid
Elderly survivors with homozygous sickle cell disease.
Dahkki: Serjeant, G, et al.
Almmustuhtton: (2007)
The interaction of alpha thalassaemia and sickle cell-beta zero thalassaemia.
Dahkki: Vyas, P, et al.
Almmustuhtton: (1988)
Are there clinical phenotypes of homozygous sickle cell disease?
Dahkki: Alexander, N, et al.
Almmustuhtton: (2004)
The red cell distribution width in sickle cell disease--is it of clinical value?
Dahkki: Thame, M, et al.
Almmustuhtton: (1991)
The changing face of homozygous sickle cell disease: 102 patients over 60 years.
Dahkki: Serjeant, G, et al.
Almmustuhtton: (2009)