Thalassemia-like phenotype in a novel complex hemoglobinopathy with α, β, δ globin chain abnormalities

Keyphrases

• Thalassemia 100%
• Hemoglobin 100%
• Hemoglobinopathies 100%
• Globin Chains 100%
• Novel Complex 100%
• Globin Genes 40%
• Anemia 20%
• Clinical Features 20%
• Heterozygote 20%
• Indian Population 20%
• Molecular Characteristics 20%
• Variant Hemoglobin 20%
• Diagnostic Challenge 20%
• Hemoglobin A2 20%
• Genotype-phenotype Correlation 20%
• African Ancestry 20%
• DNA Analysis 20%
• European Population 20%
• Laboratory Features 20%
• Thal 20%
• First Occurrence 20%
• Complex Phenotypes 20%
• Trace Amount 20%
• Thalassemia Minor 20%
• Coinheritance 20%
• Protein-based Methods 20%
• Molecular Genotype 20%
• Japanese Population 20%
• Multiple Abnormalities 20%
• Gene Abnormality 20%
• Unusual Phenotype 20%
• African American Boys 20%

Biochemistry, Genetics and Molecular Biology

• Globin 100%
• Globin Gene 50%
• Hemoglobin Variant 25%
• Hemoglobin A2 25%
• DNA Analysis 25%
• Genotype Phenotype Correlation 25%