Alpha thalassaemia phenotypes
West Indian med. j
; 17(4): 250, Dec. 1968.
Article
em En
| MedCarib
| ID: med-7550
Biblioteca responsável:
JM3.1
Localização: JM3.1; R18.W4
ABSTRACT
The effects of deficient alpha chain synthesis at the clinical and subclinical level are illustrated by observations on 17 members of a family of mixed Chinese-Scottish-Negro origins. The presence of beta thalassaemia and its variants and the haemoglobin structural mutants have been excluded by presently available methods. The family includes 5 cases of Hb H disease, 3 cases of classical alpha thalassaemia trait and two adult subjects presumed to carry "silent" alpha thalassaemia gene. Clinical and laboratory aspects are presented (AU)
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Coleções:
01-internacional
Base de dados:
MedCarib
Assunto principal:
Talassemia alfa
Limite:
Female
/
Humans
/
Male
Idioma:
En
Revista:
West Indian med. j
Ano de publicação:
1968
Tipo de documento:
Article
/
Congress and conference