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Hemoglobin D

Known as: Hb D, d hemoglobin, haemoglobin d 
National Institutes of Health

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Broader (1)

Abnormal Hemoglobins
Fifth most predominant hemoglobin:Find:Pt:Bld.dot:NomFourth most predominant hemoglobin:Find:Pt:Bld.dot:NomHemoglobins that can be presumptively identified based on available controls:Find:Pt:Bld.dot:NomMost predominant hemoglobin:Find:Pt:Bld.dot:Nom

Papers overview

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2012
2012
Hemoglobinopathies in South Gujarat population and incidence of anemia in them
OBJECTIVE: To Screen of South Gujarat population for determination of prevalence of different hemoglobinopathies particularly… 
2012
2012
HEMOGLOBIN E DISORDERS IN SOUTH GUJARAT - A STUDY OF 35 CASES
Background:Among the inherited disorders of blood, hemoglobinopathies and thalassemia constitute a major bulk of non-communicable… 
2011
2011
Co-inheritance of hemoglobin D and β-thalassemia traits in three Iranian families: clinical relevance.
Here we report the result of three cases referred to our lab that had a combination of β-thalassemia and hemoglobin D (Hb D… 
2003
2003
Crystallization and preliminary X-ray diffraction study of hemoglobin D from the Aldabra giant tortoise, Geochelone gigantea.
Hemoglobin D (Hb D) from the Aldabra giant tortoise, Geochelone gigantea, was crystallized by the hanging drop vapor diffusion… 
2002
2002
The Primary Structure of Hemoglobin D from the Aldabra Giant Tortoise, Geochelone gigantea
The complete primary structures of αD-2- and β-globin of hemoglobin D (Hb D) from the Aldabra giant tortoise, Geochelone gigantea… 
2001
2001
The β-globin genotype E121Q/W15X (cd121GAA→CAA/cd15TGG→TGA) underlines Hb D/β-(0) thalassaemia marked by domination of haemoglobin D
Abstract. Among 13,525 haemoglobin analyses performed in our laboratory we detected 21 cases of haemoglobin D (Hb D) disease… 
1999
1999
Molecular exclusion of haemoglobin SD disease by prenatal diagnosis
The most common Hb D variant, Haemoglobin D (Hb D) Los Angeles is caused by a glutamic acid to glutamine substitution at codon… 
1985
1985
Haemoglobin D-beta-thalassaemia in a German family. A double heterozygous haemoglobinopathy.
This report concerns a young woman, whose stained blood films revealed a hypochromic and microcytic red cell morphology. It could… 
1985
1985
Haemoglobin D-β-thalassaemia in a German family
SummaryThis report concerns a young woman, whose stained blood films revealed a hypochromic and microcytic red cell morphology… 
1982
1982
Neonatal screening for sickle haemoglobinopathies in Birmingham.
During 1978-81 there were about 43,500 births in Birmingham, of which 10.3% were to Negroes and 22.6% to Asians. Cellulose… 
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