International audienceHb Dompierre [β29(B11)Gly→Arg, HBB: c.88G>C] is a rare β-globin gene variant that was previously described in the heterozygous state in a 24-year-old female patient. It is defined in the HbVar database as being clinically and biologically asymptomatic. A few years after the first description, we had an opportunity of reassessing the index case because she presented with splenomegaly and clinical and biological manifestations of hemolysis. After ruling out the most common causes of hemolysis, further analyses on the variant hemoglobin (Hb) using brilliant cresyl blue staining, indicated that it showed mild instability, which may explain the clinical and biological manifestations. A structural bioinformatic analysis on t...
Hemoglobin (Hb) Hope is a rare Hb variant which is clinically silent but causes spuriously high glyc...
BACKGROUND: Hemoglobin Shepherds Bush (Human Genome Variation Society name: HBB:c.224G \u3e A) is an...
Unstable hemoglobinopathies (UHs) are rare anemia disorders (RADs) characterized by abnormal hemoglo...
International audienceHb Dompierre [β29(B11)Gly→Arg, HBB: c.88G>C] is a rare β-globin gene variant t...
An α-chain variant hemoglobin was found in the hemolysate of a 21-year-old healthy male living in Ba...
Abstract Hemoglobin (Hb) variants may be associated with low oxygen saturation and exacerbated episo...
We describe two unrelated patients, both heterozygous for an unstable hemoglobin (Hb) variant named ...
Hb variants are structurally abnormal haemoglobins which can originate a wide range of phenotypes fr...
Hemoglobinopathies are a group of inherited hemoglobin (Hb) disorders including thalassemia (reduced...
Hemoglobin structural abnormalities are among the most commonly found human genetic diseases. The La...
We report a clinical update of the hemoglobin (Hb) variant [β27(B9)Ala→Gly; HBB: c.83C>G], named Hb ...
Hemoglobinopathies, the disorders of hemoglobin structure and synthesis, can be divided into two for...
Hb H Disease is caused by the loss or inactivation of three of the four functional α-globin genes. P...
A new unstable hemoglobin (Hb) variant, named Hb Aalesund, was detected during Hb A1c measurement in...
A new unstable hemoglobin (Hb) variant, named Hb Aalesund, was detected during Hb A1c measurement in...
Hemoglobin (Hb) Hope is a rare Hb variant which is clinically silent but causes spuriously high glyc...
BACKGROUND: Hemoglobin Shepherds Bush (Human Genome Variation Society name: HBB:c.224G \u3e A) is an...
Unstable hemoglobinopathies (UHs) are rare anemia disorders (RADs) characterized by abnormal hemoglo...
International audienceHb Dompierre [β29(B11)Gly→Arg, HBB: c.88G>C] is a rare β-globin gene variant t...
An α-chain variant hemoglobin was found in the hemolysate of a 21-year-old healthy male living in Ba...
Abstract Hemoglobin (Hb) variants may be associated with low oxygen saturation and exacerbated episo...
We describe two unrelated patients, both heterozygous for an unstable hemoglobin (Hb) variant named ...
Hb variants are structurally abnormal haemoglobins which can originate a wide range of phenotypes fr...
Hemoglobinopathies are a group of inherited hemoglobin (Hb) disorders including thalassemia (reduced...
Hemoglobin structural abnormalities are among the most commonly found human genetic diseases. The La...
We report a clinical update of the hemoglobin (Hb) variant [β27(B9)Ala→Gly; HBB: c.83C>G], named Hb ...
Hemoglobinopathies, the disorders of hemoglobin structure and synthesis, can be divided into two for...
Hb H Disease is caused by the loss or inactivation of three of the four functional α-globin genes. P...
A new unstable hemoglobin (Hb) variant, named Hb Aalesund, was detected during Hb A1c measurement in...
A new unstable hemoglobin (Hb) variant, named Hb Aalesund, was detected during Hb A1c measurement in...
Hemoglobin (Hb) Hope is a rare Hb variant which is clinically silent but causes spuriously high glyc...
BACKGROUND: Hemoglobin Shepherds Bush (Human Genome Variation Society name: HBB:c.224G \u3e A) is an...
Unstable hemoglobinopathies (UHs) are rare anemia disorders (RADs) characterized by abnormal hemoglo...