Keyphrases
Sickle Cell Disease
100%
α-thalassemia
100%
α-Globin Gene
100%
β-Thalassemia (β-thal)
100%
Molecular Genetics
100%
Omani Population
100%
Pression
100%
Mean Corpuscular Volume
30%
Microcytosis
30%
Hemoglobin
30%
Thalassemia
30%
Premarital Counseling
30%
Ethics Committees
15%
α Gene
15%
Hemoglobin Electrophoresis
15%
Hypochromia
15%
Complete Blood Count
15%
Normal Blood
15%
Molecular Screening
15%
Ferritin
15%
Research Committee
15%
Microcytic Hypochromic Anemia
15%
Preimplantation Genetic Diagnosis
15%
Red Cell Distribution Width
15%
Gene Triplication
15%
Medical Ethics
15%
Nutritional Anemia
15%
CBC Test
15%
Nutritional Status
15%
Uncommon mutation
15%
Double Genes
15%
Red Blood Cells
15%
Outpatient Clinic
15%
Blood Donors
15%
Gene Dosage Analysis
15%
Clinical Behaviour
15%
Hematology
15%
Gene Deletion
15%
Molecular Features
15%
GeneScan
15%
Iron Deficiency
15%
Neonatal Screening Program
15%
Research Councils
15%
Arab Population
15%
Abnormal Hemoglobin
15%
Informed Consent
15%
Point mutation
15%
Structural Defects
15%
Anemia
15%
Strategic Projects
15%
Steady State
15%
Clinical Phenotype
15%
Executive Summary
15%
Project Proposal
15%
Patient Management
15%
Variable Frequency
15%
DNA Sequencing
15%
Medical Research
15%
Majesty
15%
Oman
15%
Medicine and Dentistry
Hemoglobin Alpha Chain
100%
Sickle-Cell Disease
100%
Alpha-Thalassemia
100%
Comprehension
100%
Beta Thalassemia
100%
Globin Gene
100%
Gene
46%
Counseling
30%
Mean Corpuscular Volume
30%
Anemia
30%
Diagnosis
30%
Analysis
30%
Screening
30%
Thalassemia
30%
Microcytosis
30%
Hemoglobin
30%
Gene Dosage
15%
DNA Sequence
15%
Gene Deletion
15%
Outpatient
15%
Medical Ethics
15%
Hematology
15%
Preimplantation Genetic Diagnosis
15%
Medical Research
15%
Hemoglobin Variant
15%
Hemoglobin Electrophoresis
15%
Erythrocyte
15%
Phenotype
15%
Iron Deficiency
15%
Nutritional Status
15%
Adult
15%
Cells
15%
High-Performance Liquid Chromatography
15%
Polymerase Chain Reaction
15%
Informed Consent
15%
Blood
15%
Diseases
15%
Steady State
15%
Patient Care
15%
Ferritin
15%
Point Mutation
15%
Newborn Screening
15%
Evaluation Study
15%
Patient
15%
Blood Donor
15%
INIS
thalassemia
100%
globins
100%
genes
100%
diseases
100%
genetics
100%
populations
100%
hemoglobin
30%
anemias
15%
volume
15%
patients
15%
screening
15%
blood count
7%
ferritin
7%
point mutations
7%
ethics
7%
width
7%
pcr
7%
blood cells
7%
oman
7%
dna sequencing
7%
management
7%
hplc
7%
steady-state conditions
7%
interactions
7%
electrophoresis
7%
hematology
7%
adults
7%
comparative evaluations
7%
detection
7%
phenotype
7%
iron
7%
defects
7%
proposals
7%
mutations
7%
distribution
7%
spectra
7%
blood
7%