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Hemoglobin D Disease

Known as: Hb D-disease, Hb-D disease 
A condition characterized by the presence of a variant of normal hemoglobin (hemoglobin D), which is caused by mutation(s) in the gene encoding the… Expand
National Institutes of Health

Papers overview

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2014
2014
Haemoglobin D (Hb D) is the fourth most common haemoglobin variant. With the exact chemical analysis of hemoglobin variants, it… Expand
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2013
2013
Introduction. Sickle cell hemoglobin D disease (HbSD) is a rare variant of sickle cell disease (SCD). Incidence of pulmonary… Expand
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Review
2010
Review
2010
Sickle cell hemoglobin D disease is a rare variant of sickle cell disease. Affected patients suffer from episodes of acute… Expand
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2003
2003
Homozygous Hb D disease is a rare disease and usually presents with mild hemolytic anemia and mild to moderate splenomegaly… Expand
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1988
1988
 
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1978
1978
A case of sickle cell Hb D disease is reported in a young Iranian male, the father of whom carried an AS sickle cell trait and… Expand
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1972
1972
 
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1971
1971
  • Rup C. Jain
  • American journal of clinical pathology
  • 1971
  • Corpus ID: 29927146
Hemoglobin D disease in a Christian family of Indian ancestry is described. A boy 10 years of age and his mother were found to… Expand
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1968
1968
Data are presented on two Caucasian families with hemoglobin D Los Angeles, (α2β2121 gln) In one family, the mother, of Spanish… Expand
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Review
1960
Review
1960
HEMOGLOBIN D was the fifth human hemoglobin to be described after hemoglobin A (normal adult), hemoglobin F (normal fetal… Expand
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