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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
11-12
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pubmed:dateCreated |
1976-2-27
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pubmed:abstractText |
The ratio of total globin alpha to beta chain synthesis was determined in reticulocytes isolated from the blood of the members of a black family, some of whom had sickle cell trait with low blood HbS concentrations (25-30%). The results support the hypothesis that sickle cell trait individuals with low HbS concentrations also carry a gene for alpha-thalassemia.
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
0006-2928
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
13
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
783-8
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:1200978-Anemia, Sickle Cell,
pubmed-meshheading:1200978-Female,
pubmed-meshheading:1200978-Hemoglobin, Sickle,
pubmed-meshheading:1200978-Hemoglobins,
pubmed-meshheading:1200978-Hemoglobins, Abnormal,
pubmed-meshheading:1200978-Humans,
pubmed-meshheading:1200978-Male,
pubmed-meshheading:1200978-Pedigree,
pubmed-meshheading:1200978-Reticulocytes,
pubmed-meshheading:1200978-Sickle Cell Trait,
pubmed-meshheading:1200978-Thalassemia
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pubmed:year |
1975
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pubmed:articleTitle |
Hemoglobin synthesis studies of a family with alpha-thalassemia trait and sickle cell trait.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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