IV. The chemical heterogeneity of the chain from human fetal hemoglobin

Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia.

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Clinical, hematological, and molecular features in Sicilians with Hb S-beta-thalassemia.

American journal of hematology·1992

Molecular characterization of beta-thalassemia in Azerbaijan.

Human genetics·1992

Black beta-thalassemia homozygotes with specific sequence variations in the 5' hypersensitive site-2 of the locus control region have high levels of fetal hemoglobin.

American journal of hematology·1992

Heterogeneity of the hemoglobin of the Ohrid trout (Salmo L. typicus).

Biochemical genetics·1992

Haplotypes in SS patients from Nigeria; characterization of one atypical beta S haplotype no. 19 (Benin) associated with elevated HB F and high G gamma levels.

Annals of hematology·1992

Problems associated with clinical chemistry quality control materials.

CRC critical reviews in clinical laboratory sciences·1980

Soluble immune complexes in human disease.

CRC critical reviews in clinical laboratory sciences·1980

Transfer factor.

CRC critical reviews in clinical laboratory sciences·1980

Structural, functional, and clinical aspects of gamma-glutamyltransferase.

CRC critical reviews in clinical laboratory sciences·1980

Screening tests for cell-mediated immunodeficiency diseases.

CRC critical reviews in clinical laboratory sciences·1979

Calcium measurements in serum and plasma--total and ionized.

CRC critical reviews in clinical laboratory sciences·1979

Argatroban Anticoagulation for Transcarotid TAVR Under Conscious Sedation in a Patient With Heparin-Induced Thrombocytopenia.

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Related Experiment Videos

IV. The chemical heterogeneity of the chain from human fetal hemoglobin

Related Concept Videos

Heterozygosity for the IVS-I-5 (G-->C) mutation with a G-->A change at codon 18 (Val-->Met; Hb Baden) in cis and a T-->G mutation at codon 126 (Val-->Gly; Hb Dhonburi) in trans resulting in a thalassemia intermedia.

Clinical, hematological, and molecular features in Sicilians with Hb S-beta-thalassemia.

Molecular characterization of beta-thalassemia in Azerbaijan.

Black beta-thalassemia homozygotes with specific sequence variations in the 5' hypersensitive site-2 of the locus control region have high levels of fetal hemoglobin.

Heterogeneity of the hemoglobin of the Ohrid trout (Salmo L. typicus).

Haplotypes in SS patients from Nigeria; characterization of one atypical beta S haplotype no. 19 (Benin) associated with elevated HB F and high G gamma levels.

Problems associated with clinical chemistry quality control materials.

Soluble immune complexes in human disease.

Transfer factor.

Structural, functional, and clinical aspects of gamma-glutamyltransferase.

Screening tests for cell-mediated immunodeficiency diseases.

Calcium measurements in serum and plasma--total and ionized.

Argatroban Anticoagulation for Transcarotid TAVR Under Conscious Sedation in a Patient With Heparin-Induced Thrombocytopenia.

Association of Life's Essential 8 With Clonal Hematopoiesis and Coronary Artery Disease.

Contemporary Analysis of the Volume-Outcome Relationship for Patients With Nontraumatic Subarachnoid Hemorrhage.

Temporal Dynamics of Complement Activation and Outcome in Patients With Acute Ischemic Stroke.

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IV. The chemical heterogeneity of the chain from human fetal hemoglobin

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