|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
3
|
|
pubmed:dateCreated |
1997-7-16
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|
pubmed:abstractText |
DNA analysis makes it possible to confirm the clinical diagnosis of the majority of cases DMD/BMD and to detect at the same time carries and the prenatal diagnosis for relatives at risk. The objective of the present work was to improve the haplotype analysis and to identify the most frequent deletions in carries.
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|
pubmed:language |
slo
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Feb
|
|
pubmed:issn |
0008-7335
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:day |
5
|
|
pubmed:volume |
136
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
90-4
|
|
pubmed:dateRevised |
2006-11-15
|
|
pubmed:meshHeading |
pubmed-meshheading:9221176-Dystrophin,
pubmed-meshheading:9221176-Female,
pubmed-meshheading:9221176-Humans,
pubmed-meshheading:9221176-Male,
pubmed-meshheading:9221176-Muscular Dystrophies,
pubmed-meshheading:9221176-Pedigree,
pubmed-meshheading:9221176-Polymerase Chain Reaction,
pubmed-meshheading:9221176-Polymorphism, Genetic,
pubmed-meshheading:9221176-Repetitive Sequences, Nucleic Acid,
pubmed-meshheading:9221176-Sequence Deletion
|
|
pubmed:year |
1997
|
|
pubmed:articleTitle |
[Use of CA repeat polymorphism in direct and indirect diagnosis of Duchenne and Becker muscular dystrophy].
|
|
pubmed:affiliation |
Odd. klinické genetiky I, FN Motol, Praha.
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|
pubmed:publicationType |
Journal Article,
English Abstract
|
