Source:http://linkedlifedata.com/resource/pubmed/id/19668304
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
|
pubmed:dateCreated |
2009-8-11
|
pubmed:abstractText |
Autosomal Dominant Polycystic Kidney Disease (ADPKD) is the most common life-threatening hereditary disease. Molecular analysis with highly polymorphic short tandem repeats, located in the vicinity of the two genes responsible for the disease (PKD1 and PKD2), is used to confirm diagnosis and give genetic counseling to members of affected families.
|
pubmed:language |
spa
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:issn |
0211-6995
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:volume |
29
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
327-30
|
pubmed:meshHeading |
pubmed-meshheading:19668304-Female,
pubmed-meshheading:19668304-Humans,
pubmed-meshheading:19668304-Male,
pubmed-meshheading:19668304-Microsatellite Repeats,
pubmed-meshheading:19668304-Polycystic Kidney, Autosomal Dominant,
pubmed-meshheading:19668304-Polymerase Chain Reaction,
pubmed-meshheading:19668304-TRPP Cation Channels
|
pubmed:year |
2009
|
pubmed:articleTitle |
[Genetic diagnosis of autosomal dominant polycystic kidney disease using multiplex-PCR].
|
pubmed:affiliation |
Unidad de Investigación, Las Palmas de Gran Canaria.
|
pubmed:publicationType |
Journal Article,
English Abstract
|