Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
1
|
| pubmed:dateCreated |
1984-10-23
|
| pubmed:abstractText |
In this study we have correlated the presence/absence of rare red blood cells with HbH inclusions with the alpha-globin genotype in a group of Sardinian alpha-thalassemia carriers, whose genotype have been defined by alpha-globin gene mapping. We found that the majority of the carriers investigated, including those with the deletion of a single or two alpha-globin genes and those with non-deletion lesions, have rare blood cells with inclusions, with no significant difference in the frequency of positive finding related to the alpha-globin genotype.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0001-5792
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
72
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
34-6
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:6089487-Adult,
pubmed-meshheading:6089487-Female,
pubmed-meshheading:6089487-Genotype,
pubmed-meshheading:6089487-Globins,
pubmed-meshheading:6089487-Hemoglobin H,
pubmed-meshheading:6089487-Hemoglobins, Abnormal,
pubmed-meshheading:6089487-Heterozygote,
pubmed-meshheading:6089487-Humans,
pubmed-meshheading:6089487-Inclusion Bodies,
pubmed-meshheading:6089487-Mediterranean Islands,
pubmed-meshheading:6089487-Pregnancy,
pubmed-meshheading:6089487-Thalassemia
|
| pubmed:year |
1984
|
| pubmed:articleTitle |
Hemoglobin inclusions in heterozygous alpha-thalassemia according to their alpha-globin genotype.
|
| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|