Hemoglobin H Disease

Known as: HEMOGLOBIN H DISEASE, DELETIONAL, ALPHA-THALASSEMIA, HEMOGLOBIN H TYPE, Hemoglobin H 
A form of alpha thalassemia that results from reduced protein production from three of the four alpha-globin genes. Clinically it is characterized by… (More)
National Institutes of Health

Papers overview

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Highly Cited
2003
Highly Cited
2003
Most introns of archaeal tRNA genes (tDNAs) are located in the anticodon loop, between nucleotides 37 and 38, the unique location… (More)
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Highly Cited
2001
Highly Cited
2001
Frequently, crop plants do not take up adequate amounts of iron from the soil, leading to chlorosis, poor yield and decreased… (More)
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2001
2001
Definitive diagnosis of concurrent hemoglobin (Hb) H disease and heterozygous beta-thalassemia cannot be made from Hb analysis… (More)
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Highly Cited
2000
Highly Cited
2000
BACKGROUND Normally, one pair of each of the two alpha-globin genes, alpha1 and alpha2, resides on each copy of chromosome 16. In… (More)
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1997
1997
Hemoglobin Constant Spring (HbCS) is the most common nondeletional alpha-thalassemic mutation and is an important cause of HbH… (More)
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Review
1995
Review
1995
The hallmarks of the X-linked alpha-thalassemia/mental retardation (ATR-X) syndrome are severe psychomotor retardation, minor… (More)
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1985
1985
Studies of the ability of Plasmodium falciparum to grow in vitro in the red blood cells of subjects with certain beta-thalassemia… (More)
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1983
1983
The presence of hemoglobin H (beta 4), resulting from a deficiency of alpha-globin chain synthesis, was observed as an acquired… (More)
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1973
1973
Functional messenger RNA (mRNA) for human globin synthesis was isolated from reticulocytes of each of two patients with… (More)
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1961
1961
With the Technical Assistance of George Cummings, Marze L. Duersl1 Donald R. Maim, Katherine Swisher and Patricia Vanbeilinghen S… (More)
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