Keyphrases
Genetic Characteristics
100%
Clinical Characteristics
100%
Oman
100%
Heterozygote
28%
Compound Heterozygous mutation
28%
Thalassemia
28%
Hemoglobinopathies
14%
Soman
14%
Hypersplenism
14%
Globin Genes
14%
Phenotype Modifiers
14%
Clinical Syndromes
14%
Blood Transfusion
14%
Disease Entity
14%
Transfusion-dependent Thalassemia
14%
Early Infancy
14%
Clinical Manifestations
14%
Clinical Phenotype
14%
β-Thalassemia (β-thal)
14%
Severe Disease
14%
Sickle Cell Disease
14%
INIS
genetics
100%
oman
100%
diseases
100%
heterozygotes
57%
carriers
42%
thalassemia
42%
mutations
28%
transfusions
28%
phenotype
28%
boron 6
14%
genes
14%
globins
14%
blood
14%
Medicine and Dentistry
Genetic Trait
100%
Tramadol
100%
Diseases
100%
Thalassemia
40%
Thalassemia Major
20%
Sickle-Cell Disease
20%
Clinical Syndrome
20%
Hypersplenism
20%
Heterozygote
20%
Blood Transfusion
20%
Infancy
20%
Soman
20%
Hemoglobinopathy
20%
Globin Gene
20%