Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
|
pubmed:dateCreated |
1983-9-9
|
pubmed:abstractText |
We have defined a new type of delta-thalassemia in which beta-globin chain synthesis is incompletely suppressed. Homozygotes have unusually low HbA2 levels, and double heterozygosity for this delta-thalassemia gene and beta-thalassemia normalizes the HbA2 level. The delta-thalassemia occurs on a chromosome that is identifiable using polymorphic restriction endonuclease sites. We call this condition delta +-thalassemia, to distinguish it from the previously described delta 0-thalassemia syndromes in which no delta-globin chain synthesis occurs.
|
pubmed:grant | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
0006-4971
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
62
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
341-5
|
pubmed:dateRevised |
2007-11-14
|
pubmed:meshHeading |
pubmed-meshheading:6307432-Chromosome Mapping,
pubmed-meshheading:6307432-DNA Restriction Enzymes,
pubmed-meshheading:6307432-Hemoglobin A2,
pubmed-meshheading:6307432-Hemoglobins, Abnormal,
pubmed-meshheading:6307432-Heterozygote,
pubmed-meshheading:6307432-Homozygote,
pubmed-meshheading:6307432-Humans,
pubmed-meshheading:6307432-Italy,
pubmed-meshheading:6307432-Male,
pubmed-meshheading:6307432-Pedigree,
pubmed-meshheading:6307432-Thalassemia
|
pubmed:year |
1983
|
pubmed:articleTitle |
Delta +-thalassemia in Sardinia.
|
pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
|