Pages that link to "Q48022425"

The following pages link to Hemoglobin Kenya, the product of fusion of γ and β polypeptide chains (Q48022425):

Displaying 50 items.

• G gamma beta + type of hereditary persistence of fetal haemoglobin in association with Hb C (Q33584608) (← links)
• G gamma delta beta thalassaemia and g gamma HPFH (Hb Kenya type): comparison of 2 new cases (Q33587659) (← links)
• Haemoglobin Lepore Boston-Washington in Sicily: clinical, haematological, and biosynthetic studies. (Q33667969) (← links)
• Hemoglobin Lincoln Park: a betadelta fusion (anti-Lepore) variant with an amino acid deletion in the delta chain-derived segment (Q33968895) (← links)
• Assignment of human beta-, gamma-, and delta-globin genes to the short arm of chromosome 11 by chromosome sorting and DNA restriction enzyme analysis (Q33981413) (← links)
• Recent developments in foetal haemoglobin research (Q34056437) (← links)
• Hereditary persistence of fetal haemoglobin (Q34064704) (← links)
• Hereditary persistence of foetal haemoglobin with β-chain synthesis in cis position (Gγ-β+-HPFH) in a negro family (Q34162374) (← links)
• An Individual with Hb‐Lepore‐Baltimore‐ δβ‐Thalassaemia in a Yugoslavian Family (Q34176233) (← links)
• Clinical course and molecular characterization of a compound heterozygote for sickle hemoglobin and hemoglobin kenya (Q34210780) (← links)
• The genetic control of protein synthesis: The haemoglobin model (Q34302943) (← links)
• Human globin gene expression and linkage in bone marrow and fetal liver (Q35067422) (← links)
• Human globin gene analysis for a patient with beta-o/delta beta-thalassemia (Q35081817) (← links)
• The thalassemias: molecular mechanisms of human genetic disease. (Q35202896) (← links)
• Multiple arrangements of the human embryonic zeta globin genes (Q35531471) (← links)
• Hemoglobin Kenya, the product of a gamma-beta fusion gene: studies of the family (Q35570254) (← links)
• Gamma thalassemia resulting from the deletion of a gamma-globin gene (Q35679091) (← links)
• Globin chain synthesis in single erythroid bursts from cord blood: studies on gamma leads to beta and G gamma leads to A gamma switches. (Q36352080) (← links)
• Characterization of Deletions of the HBA and HBB Loci by Array Comparative Genomic Hybridization (Q36468778) (← links)
• δβ Thalassemia and Hereditary Persistence of Fetal Hemoglobin (Q36670384) (← links)
• Compound heterozygosity for Hb S and the hybrid HbS Lepore, P-Nilotic, and Kenya; comparison of hematological and hemoglobin composition data (Q36859267) (← links)
• Hemoglobin Grady: The First Example of a Variant with Elongated Chains Due to an Insertion of Residues (Q37457217) (← links)
• The emerging complexity of genetic control of persistent fetal hemoglobin biosynthesis in adults (Q38206754) (← links)
• Fusion genes in malignant neoplastic disorders of haematopoietic system (Q38731027) (← links)
• The Kenya Form of Hereditary Persistence of Fetal Haemoglobin: Structural Studies and Evidence for Homogeneous Distribution of Haemoglobin F using Fluorescent Anti‐haemoglobin F Antibodies (Q38893650) (← links)
• Hemoglobin Chapel Hill or alpha2 74 Asp replaced by Gly beta2 (Q39107843) (← links)
• Hereditary persistence of fetal haemoglobin (HPFH) and delta beta thalassaemia (Q39584333) (← links)
• The Human γ-Chain Variants: A Review (Q39708724) (← links)
• Recent developments in the molecular genetics of human hemoglobin (Q39798627) (← links)
• DNA polymorphism and molecular pathology of the human globin gene clusters (Q39813814) (← links)
• The potential molecular mechanism of thalassemias and related disorders (Q39949559) (← links)
• The Synthesis and Chemical Heterogeneity of Human Fetal Hemoglobin: Overview and present concepts (Q40098676) (← links)
• Mapping of the human globin genes (Q40099228) (← links)
• The molecular basis of disorders of human hemoglobin synthesis (Q40122684) (← links)
• Human Haemoglobin Genetics (Q40437524) (← links)
• Structure of the human fetal globin gene locus (Q41461227) (← links)
• Biosynthetic and structural studies of hemoglobin in a patient with congenital dyserythropoietic anemia type I. (Q41467060) (← links)
• Gene Deletion as the Molecular Basis for the Kenya-Gγ-Hpfh Condition (Q41544225) (← links)
• Recombination Hot Spots and Human Disease (Q41574990) (← links)
• Globin gene deletion in HPFH, δ°β° thalassaemia and Hb Lepore disease (Q41644742) (← links)
• Characterisation of deletions which affect the expression of fetal globin genes in man (Q41644946) (← links)
• The Structure of Goat Hemoglobins V. A Fourth β Chain Variant (β-D-Malta; 69 Asp ↠ Gly) with Decreased Oxygen Affinity and Occurring at a High Frequency in Malta (Q41685531) (← links)
• The hemoglobin P-Galveston-Hb-C conduction in members of a black family from South Carolina (Q43703229) (← links)
• Hemoglobins Lepore and anti-Lepore (Q43767400) (← links)
• A > 200 kb deletion removing the entire β-like globin gene cluster in a family of Irish Descent (Q44511891) (← links)
• A second patient with hemoglobin Alberta, a high-oxygen-affinity variant causing erythrocytosis and forming asymmetric tetramers (Q44555737) (← links)
• Hemoglobin Alamo (alpha2beta2 19 (b1) Asn replaced by Asp) (Q44823092) (← links)
• Hb Kenya among Luo adults and young children in malaria holoendemic Western Kenya: screened by high performance liquid chromatography and confirmed by polymerase chain reaction (Q44881241) (← links)
• A form of hereditary persistence of fetal haemoglobin characterized by uneven cellular distribution of haemoglobin F and the production of haemoglobins A and A2 in homozygotes (Q45218360) (← links)
• Identification of Hb Kenya (Agamma81Leu-beta86Ala) by electrospray mass spectrometry (Q46703484) (← links)