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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
1
|
| pubmed:dateCreated |
1985-6-18
|
| pubmed:abstractText |
Epidemiologic programs in Martinique during the last 10 years and particularly the last 5, have allowed the determination of the Hb S, Hb C, beta thalassemia traits frequencies. A number of rare variants have been detected during the course of these screening programs. Many of these Hb variants have been analysed at the structural level. For some of them a pathologic interaction with Hb S is observed (Hb D Punjab, Hb O Arab...), and the use of electrophoretic mobilities obtained with the reference samples provides the basis of a rapid, highly probable presumptive identification and then, a useful tool, when for example genetic counselling is necessary.
|
| pubmed:language |
fre
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:author | |
| pubmed:volume |
27
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
11-4
|
| pubmed:dateRevised |
2006-11-15
|
| pubmed:meshHeading |
pubmed-meshheading:3991355-Epidemiologic Methods,
pubmed-meshheading:3991355-Hemoglobin, Sickle,
pubmed-meshheading:3991355-Hemoglobin C,
pubmed-meshheading:3991355-Hemoglobins, Abnormal,
pubmed-meshheading:3991355-Humans,
pubmed-meshheading:3991355-Infant, Newborn,
pubmed-meshheading:3991355-Isoelectric Focusing,
pubmed-meshheading:3991355-Martinique,
pubmed-meshheading:3991355-Phenotype,
pubmed-meshheading:3991355-Sickle Cell Trait,
pubmed-meshheading:3991355-Thalassemia
|
| pubmed:year |
1985
|
| pubmed:articleTitle |
[Abnormal hemoglobins identified in Martinique].
|
| pubmed:publicationType |
Journal Article,
English Abstract
|