Beta talasemia mayor en la Argentina / [Beta thalassemia major in Argentina]
Medicina (B.Aires)
; 62(2): 124-134, 2002.
Article
in Es
| LILACS, BINACIS
| ID: biblio-1165117
Responsible library:
BR1.1
Localization: [{"text": "AR2.1"}]
ABSTRACT
An analysis of beta thalassemia major patients seen at Hospital Juan P. Garrahan was carried out in order to determine the characteristics and outcome of the population. From August 1987 to July 2000, 45 patients were admitted (27 males-18 females). The most common beta globin gene defects were C-39 (30.7
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Collection:
01-internacional
Database:
BINACIS
/
LILACS
Main subject:
Genetic Testing
/
Beta-Thalassemia
/
Mutation
Type of study:
Observational_studies
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Child
/
Child, preschool
/
Female
/
Humans
/
Infant
/
Male
Country/Region as subject:
America do sul
/
Argentina
Language:
Es
Journal:
Medicina (B.Aires)
Journal subject:
MEDICINA
Year:
2002
Document type:
Article
Country of publication:
Argentina