Alpha trait thalassemia

Known as: ALPHA-THALASSEMIA TRAIT, Alpha Thalassemia Trait

A condition in which a person has reduced protein production from two of the four alpha-globin alleles.

National Institutes of Health

Papers overview

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2019

OZET Trombositoz siklikla rastlantisal olarak karsimiza cikan ancak ayirici tanisi onemli olan bir bulgudur. Modern hematoloji…

2016

Thalassemia syndromes are the most common hereditary genetic diseases of mankind. They result from an imbalance between the…

2004

To investigate the clinical application of multiplex PCR in detecting genotypes of deletional alpha-thalassemia in South China…

1985

Modification de la technique au bleu de methylene permettant de deceler des inclusions intra-erythrocytaires chez les patients…

1985

Restriction enzyme analysis of the alpha and zeta globin genes was carried out in four cases of Hb Bart's hydrops fetalis, in…

1981

The frequency of alpha thalassemia in SR Macedonia was determined with studies of Hb Bart's in 1.140 newborn babies. Hb Bart's…

1979

A 3-year-old child of Sicilian origin was found to have a severe form of Cooley's anemia. Investigations were extended to other…

1977

The frequency of thalassemia was determined in a group of 541 healthy adult black males. Individuals with decreased mean…

1976

The alpha thalassemias are associated with a decrease in alpha chain synthesis. Hemoglobin H (HbH) disease is a moderately severe…

1976

The alpha thalassemias are associated with a decrease in alpha chain synthesis. Hemoglobin H (HbH) disease is a moderately severe…