Hemoglobin Bart's disease in an Italian boy. Interaction between alpha-thalassemia and hereditary persistence of fetal hemoglobin.

Translocation of an erythroid-specific hypersensitive site in deletion-type hereditary persistence of fetal hemoglobin.

Hereditary persistence of fetal hemoglobin, beta thalassemia, and the hemoglobin delta-beta locus: further family data and genetic interpretations.

Featured Article: Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting microRNAs.

BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterations.

Inheritance of F cell frequency in heterocellular hereditary persistence of fetal hemoglobin: an example of allelic exclusion.

Absence of messenger RNA and gene DNA for beta-globin chains in hereditary persistence of fetal hemoglobin.

A G gamma type of the hereditary persistence of fetal hemoglobin with beta chain production in cis.

Hemoglobin interacting proteins and implications of spectrin hemoglobin interaction.

Fetal hemoglobin levels in SIDS.

An improved chromatographic procedure for quantitation of human fetal hemoglobin.

Genome-wide analysis of aberrantly expressed lncRNAs and miRNAs with associated co-expression and ceRNA networks in β-thalassemia and hereditary persistence of fetal hemoglobin.

Detection of fetal hemoglobin in stool specimens and differentiation from maternal hemoglobin.

Fetal hemoglobin in sickle cell anemia.

The Bessis reticular cell, the hemoglobin 'switch' and the role of fetal hemoglobin: a hypothesis.

Hemoglobin ontogeny during normal mouse fetal development.

MR Imaging-derived Oxygen-Hemoglobin Dissociation Curves and Fetal-Placental Oxygen-Hemoglobin Affinities.

Hemoglobin C disease.

Hemoglobin switching's surprise: the versatile transcription factor BCL11A is a master repressor of fetal hemoglobin.

Two novel mutations (HBG1: c.-250C > T and HBG2: c.-250C > T) associated with hereditary persistence of fetal hemoglobin.

Neonatal screening for α-thalassemia by cord hemoglobin Barts: how effective is it?

Interaction of butene with human hemoglobin A.

Fetal hemoglobin and alpha-fetoprotein in various malignancies.

Heme synthesis in hereditary hemolytic anemias: decreased delta-aminolevulinic acid synthetase in hemoglobin Köln disease.

Hereditary persistence of fetal haemoglobin (HPFH) and delta beta thalassaemia.

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Translocation of an erythroid-specific hypersensitive site in deletion-type hereditary persistence of fetal hemoglobin.

Hereditary persistence of fetal hemoglobin, beta thalassemia, and the hemoglobin delta-beta locus: further family data and genetic interpretations.

Featured Article: Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian δβ-thalassemia, by BCL11A and SOX6-targeting microRNAs.

BCL11A deletions result in fetal hemoglobin persistence and neurodevelopmental alterations.

Inheritance of F cell frequency in heterocellular hereditary persistence of fetal hemoglobin: an example of allelic exclusion.

Absence of messenger RNA and gene DNA for beta-globin chains in hereditary persistence of fetal hemoglobin.

A G gamma type of the hereditary persistence of fetal hemoglobin with beta chain production in cis.

Hemoglobin interacting proteins and implications of spectrin hemoglobin interaction.

Fetal hemoglobin levels in SIDS.

An improved chromatographic procedure for quantitation of human fetal hemoglobin.

Genome-wide analysis of aberrantly expressed lncRNAs and miRNAs with associated co-expression and ceRNA networks in β-thalassemia and hereditary persistence of fetal hemoglobin.

Detection of fetal hemoglobin in stool specimens and differentiation from maternal hemoglobin.

Fetal hemoglobin in sickle cell anemia.

The Bessis reticular cell, the hemoglobin 'switch' and the role of fetal hemoglobin: a hypothesis.

Hemoglobin ontogeny during normal mouse fetal development.

MR Imaging-derived Oxygen-Hemoglobin Dissociation Curves and Fetal-Placental Oxygen-Hemoglobin Affinities.

Hemoglobin C disease.

Hemoglobin switching's surprise: the versatile transcription factor BCL11A is a master repressor of fetal hemoglobin.

Two novel mutations (HBG1: c.-250C > T and HBG2: c.-250C > T) associated with hereditary persistence of fetal hemoglobin.

Neonatal screening for α-thalassemia by cord hemoglobin Barts: how effective is it?

Interaction of butene with human hemoglobin A.

Fetal hemoglobin and alpha-fetoprotein in various malignancies.

Heme synthesis in hereditary hemolytic anemias: decreased delta-aminolevulinic acid synthetase in hemoglobin Köln disease.

Hereditary persistence of fetal haemoglobin (HPFH) and delta beta thalassaemia.

Hemoglobin Bart's disease in an Italian boy. Interaction between alpha-thalassemia and hereditary persistence of fetal hemoglobin.

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