SummaryFetal hemoglobin (Hb F) and fetal cell (FC) levels in adults show considerable variation and are influenced by several genetic variants; the major determinants appear to be unlinked to the β-globin gene cluster. Recently, a trans-acting locus controlling Hb F and FC production has been mapped to chromosome 6q23 in an Asian Indian kindred that includes individuals with heterocellular hereditary persistence of Hb F (HPFH) associated with β thalassemia. We have extended the kindred by 57 members, bringing the total studied to 210, and have saturated the region with 26 additional markers. Linkage analysis showed tight linkage of the quantitative-trait locus (QTL) to the anonymous markers D6S976 (LOD score 11.3; recombination fraction .00...
Fetal haemoglobin (HbF) is a major ameliorating factor in sickle cell disease. We investigated if a ...
Fetal haemoglobin (HbF) is a major ameliorating factor in sickle cell disease. We investigated if a ...
We report a study of four families of Italian origin in which heterocellular HPFH is inherited linke...
SummaryFetal hemoglobin (Hb F) and fetal cell (FC) levels in adults show considerable variation and ...
Individual variation in fetal hemoglobin (HbF, alpha(2)gamma(2)) response underlies the remarkable d...
Background: Fetal haemoglobin (HbF) level modifies the clinical severity of HBB disorders. Intergeni...
"Heterocellular hereditary persistence of fetal hemoglobin" (HPFH) is the term used to describe the ...
Abstract Background Heterocellular hereditary persistence of fetal hemoglobin (HPFH) is a common mul...
Human hemoglobin genes are located in α and β globin gene clusters in chromosomes 16 and 11, respect...
In patients with sickle cell anemia, fetal hemoglobin (HbF) concentrations vary by 2 orders of magni...
During human development, the switch from fetal to adult hemoglobin (Hb) is not complete with the re...
Fetal haemoglobin (HbF) is a major ameliorating factor in sickle cell disease. We investigated if a ...
We genotyped single nucleotide polymorphisms (SNPs) in: (1) the β-globin gene-like cluster, (2) quan...
Nondeletional hereditary persistence of fetal hemoglobin (nd-HPFH), a rare hereditary condition resu...
Fetal hemoglobin (Hb F), formed by two alpha globin chains (α) and two gamma chains (γ) (α2 γ2), has...
Fetal haemoglobin (HbF) is a major ameliorating factor in sickle cell disease. We investigated if a ...
Fetal haemoglobin (HbF) is a major ameliorating factor in sickle cell disease. We investigated if a ...
We report a study of four families of Italian origin in which heterocellular HPFH is inherited linke...
SummaryFetal hemoglobin (Hb F) and fetal cell (FC) levels in adults show considerable variation and ...
Individual variation in fetal hemoglobin (HbF, alpha(2)gamma(2)) response underlies the remarkable d...
Background: Fetal haemoglobin (HbF) level modifies the clinical severity of HBB disorders. Intergeni...
"Heterocellular hereditary persistence of fetal hemoglobin" (HPFH) is the term used to describe the ...
Abstract Background Heterocellular hereditary persistence of fetal hemoglobin (HPFH) is a common mul...
Human hemoglobin genes are located in α and β globin gene clusters in chromosomes 16 and 11, respect...
In patients with sickle cell anemia, fetal hemoglobin (HbF) concentrations vary by 2 orders of magni...
During human development, the switch from fetal to adult hemoglobin (Hb) is not complete with the re...
Fetal haemoglobin (HbF) is a major ameliorating factor in sickle cell disease. We investigated if a ...
We genotyped single nucleotide polymorphisms (SNPs) in: (1) the β-globin gene-like cluster, (2) quan...
Nondeletional hereditary persistence of fetal hemoglobin (nd-HPFH), a rare hereditary condition resu...
Fetal hemoglobin (Hb F), formed by two alpha globin chains (α) and two gamma chains (γ) (α2 γ2), has...
Fetal haemoglobin (HbF) is a major ameliorating factor in sickle cell disease. We investigated if a ...
Fetal haemoglobin (HbF) is a major ameliorating factor in sickle cell disease. We investigated if a ...
We report a study of four families of Italian origin in which heterocellular HPFH is inherited linke...