|
|
|
Volumn 49, Issue 6, 1999, Pages 667-674
|
|
Thalassaemia, sickle cell disease;Thalassemie, drepanocytose
a
a
HÔPITAL TENON
(France)
|
|
Author keywords
[No Author keywords available]
|
|
Indexed keywords
GLOBIN;
HEMOGLOBIN;
ALPHA THALASSEMIA;
ANEMIA;
BETA THALASSEMIA;
BLOOD VESSEL OCCLUSION;
CLINICAL FEATURE;
GENETIC PREDISPOSITION;
HEMOLYSIS;
HERITABILITY;
HUMAN;
PATHOPHYSIOLOGY;
REVIEW;
SICKLE CELL ANEMIA;
SYMPTOM;
THALASSEMIA;
ARTICLE;
CHROMOSOME 16;
DIFFERENTIAL DIAGNOSIS;
GENETICS;
HEMOLYTIC ANEMIA;
INCIDENCE;
METABOLISM;
PHENOTYPE;
ANEMIA, HEMOLYTIC;
ANEMIA, SICKLE CELL;
CHROMOSOMES, HUMAN, PAIR 16;
DIAGNOSIS, DIFFERENTIAL;
HEMOGLOBINS;
HUMANS;
INCIDENCE;
PHENOTYPE;
THALASSEMIA;
|
|
EID: 0033559480
PISSN: 00352640
EISSN: None
Source Type: Journal
DOI: None Document Type: Review |
|
Times cited : (4)
|
|
References (0)
|
