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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
2
|
| pubmed:dateCreated |
1984-9-19
|
| pubmed:abstractText |
Two types of alpha+ thalassemia (-alpha l) have been described, respectively termed leftward and rightward, which correspond to nonhomologous crossing-over in different homology zones X and Z within the alpha-globin gene cluster. Up to now the leftward type has been described only in Asiatic populations, whereas the rightward type is universally distributed. We report here a first case of leftward deletion observed in a Sicilian male. This raises the question of an identical or not crossing-over event.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0340-6717
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
67
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
216-8
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:6745942-Aged,
pubmed-meshheading:6745942-Crossing Over, Genetic,
pubmed-meshheading:6745942-Genes,
pubmed-meshheading:6745942-Globins,
pubmed-meshheading:6745942-Heterozygote,
pubmed-meshheading:6745942-Humans,
pubmed-meshheading:6745942-Male,
pubmed-meshheading:6745942-Sicily,
pubmed-meshheading:6745942-Thalassemia
|
| pubmed:year |
1984
|
| pubmed:articleTitle |
A leftward deletional alpha+ thalassemia found in East Sicily in conjunction with heterozygous beta-thalassemia.
|
| pubmed:publicationType |
Journal Article,
Case Reports,
Research Support, Non-U.S. Gov't
|