Pages that link to "Q72413050"
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The following pages link to The pattern of disordered haemoglobin synthesis in homozygous and heterozygous beta-thalassaemia (Q72413050):
Displaying 50 items.
- Loss of alpha-hemoglobin-stabilizing protein impairs erythropoiesis and exacerbates beta-thalassemia (Q28510933) (← links)
- G gamma beta + type of hereditary persistence of fetal haemoglobin in association with Hb C (Q33584608) (← links)
- Globin chain synthesis in sickle beta-thalassaemic bone marrow and reticulocytes (Q33584614) (← links)
- Homozygous beta thalassaemia in Liberia (Q33586487) (← links)
- G gamma delta beta thalassaemia and g gamma HPFH (Hb Kenya type): comparison of 2 new cases (Q33587659) (← links)
- Thalassaemia intermedia in a family with beta 0-thalassaemia and Hb Hasharon (Q33669999) (← links)
- Globin synthesis in fractionated Normoblasts of beta-thalassemia heterozygotes (Q34475312) (← links)
- Free alpha-globin pool in human bone marrow (Q34515016) (← links)
- Human globin gene analysis for a patient with beta-o/delta beta-thalassemia (Q35081817) (← links)
- Imbalanced globin chain synthesis in heterozygous beta-thalassemic bone marrow (Q35090458) (← links)
- Microcytosis, iron deficiency, and thalassaemia in preschool children (Q35624675) (← links)
- Molecular analysis of the beta-thalassemia phenotype associated with inheritance of hemoglobin E (alpha 2 beta2(26)Glu leads to Lys). (Q37000859) (← links)
- Globin chain synthesis in myelodysplastic syndromes (Q37144945) (← links)
- Effect of isoniazid, a haem inhibitor, on globin chain synthesis in reticulocytes from non-thalassaemic and beta thalassaemic subjects (Q37245839) (← links)
- Alpha-beta thalassaemia (Q39433917) (← links)
- Preliminary surveys for the prevalence of the thalassaemia genes in some African populations (Q39582465) (← links)
- Occurrence ofGγ Hb F in Greek HPFH: Analysis of Heterozygotes and Compound Heterozygotes with β Thalassaemia (Q39584339) (← links)
- The potential molecular mechanism of thalassemias and related disorders (Q39949559) (← links)
- The Molecular Basis of Thalassemi (Q39951141) (← links)
- Thalassemic hemoglobinopathies (Q40165274) (← links)
- Synthesis of hemoglobin Gun Hill: increased synthesis of the heme-free beta-GH globin chain and subunit exchange with a free alpha-chain pool (Q40324370) (← links)
- Molecular basis for acquired haemoglobin H disease (Q40502126) (← links)
- Acquired Haemoglobin H Disease in Leukaemia: Pathophysiology and Molecular Basis (Q40524236) (← links)
- Deficient heme synthesis as the cause of noninducibility of hemoglobin synthesis in a friend erythroleukemia cell line (Q40599838) (← links)
- Abnormal hemoglobin synthesis in some leukemic patients (Q41069843) (← links)
- An assessment of techniques suitable for the diagnosis of sickle-cell disease and haemoglobin C disease in cord blood samples (Q41252056) (← links)
- The Importance of the Genetic Picture and Globin Synthesis in Determining the Clinical and Haematological Features of Thalassaemia Intermedia (Q41481728) (← links)
- Hemoglobin constant spring: Hemoglobin synthesis in heterozygous and homozygous states (Q41864416) (← links)
- Assay of Thalassaemic Messenger RNA in the Wheat Germ System (Q43815501) (← links)
- Haemoglobin J Tongariki is associated with alpha thalassaemia (Q44459825) (← links)
- Biosynthetic Ratio of Labelled Globin Chains in Human Reticulocytes, Determined by Electrophoresis on Cellulose Acetate (Q44698164) (← links)
- Haemoglobin synthesis in 28 obligatory cases for ?-thalassemia traits (Q44984565) (← links)
- Abnormality of separate subunits of factor VIII? (Q45890207) (← links)
- Hb F Synthesis in Sickle Cell Anaemia: a Comparison of Saudi Arab Cases with those of African Origin (Q46222871) (← links)
- The interaction of hemoglobin O Arab with Hb S and beta+ thalassemia among Israeli Arabs (Q46570675) (← links)
- Haemoglobin Constant Spring--a chain termination mutant? (Q47732892) (← links)
- Adrenal glands in beta-thalassemia major: magnetic resonance (MR) imaging features and correlation with iron stores. (Q51967335) (← links)
- Maternal synthesis of haemoglobin F in pregnancy. (Q53680821) (← links)
- The control of globin synthesis in rabbit reticulocytes (Q53906661) (← links)
- Pathophysiology of thalassemias (Q54288193) (← links)
- Thalassaemia in the British. (Q54341385) (← links)
- Presence of gene for β globin in homozygous β0 thalassaemia (Q59058350) (← links)
- Defective synthesis of HbE is due to reduced levels of βE mRNA (Q59087009) (← links)
- Congenital dyserythropoietic anemia type I: Report of a pair of siblings in Japan (Q66921429) (← links)
- Globin Chain Synthesis in the Greek Type (Aγ) of Hereditary Persistence of Fetal Haemoglobin (Q67348768) (← links)
- Haemoglobin Bart's in Saudi Arabia (Q67428027) (← links)
- Foetal erythropoiesis in human leukaemia (Q67513244) (← links)
- Switch from foetal to adult haemoglobin synthesis in normal and hypophysectomised sheep (Q68237874) (← links)
- Defect in hemoglobin synthesis possibly due to a disturbed association (Q68788989) (← links)
- Haemoglobin Synthesis during Erythroid Maturation in β-Thalassaemia (Q69006905) (← links)