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| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
4
|
| pubmed:dateCreated |
1992-7-9
|
| pubmed:abstractText |
Being an X-linked condition, the sisters of men with X-linked agammaglobulinaemia have a 50% risk of being carriers of the disease gene (provided the disease has not developed as a results of a new mutation). We demonstrate how this risk can be modified very significantly by DNA analysis using linked DNA probes. The value of such tests for genetic purposes is discussed.
|
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical | |
| pubmed:status |
MEDLINE
|
| pubmed:issn |
0332-3102
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:volume |
84
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
116-8
|
| pubmed:dateRevised |
2010-11-18
|
| pubmed:meshHeading |
pubmed-meshheading:1817116-Adult,
pubmed-meshheading:1817116-Agammaglobulinemia,
pubmed-meshheading:1817116-DNA Probes,
pubmed-meshheading:1817116-Female,
pubmed-meshheading:1817116-Genetic Linkage,
pubmed-meshheading:1817116-Heterozygote Detection,
pubmed-meshheading:1817116-Humans,
pubmed-meshheading:1817116-Ireland,
pubmed-meshheading:1817116-Male,
pubmed-meshheading:1817116-Pedigree,
pubmed-meshheading:1817116-X Chromosome
|
| pubmed:articleTitle |
Carrier detection for X-linked agammaglobulinaemia (Bruton type) in an Irish family using linked DNA probes.
|
| pubmed:affiliation |
I. Mothercare Department of Paediatric Genetics, Institute of Child Health, London.
|
| pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|