|
rdf:type |
|
|
lifeskim:mentions |
|
|
pubmed:issue |
4
|
|
pubmed:dateCreated |
1998-6-25
|
|
pubmed:abstractText |
Rett syndrome in 32 children (31 girls and 1 boy) was diagnosed according to International association on Rett syndrome. The phenomenon of the presence of special type of late-replicating chromosome X (type C) was revealed. This phenomenon may be recommended as a diagnostic test for both preclinical periods of development of the disease and in atypical cases of Rett syndrome.
|
|
pubmed:language |
rus
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:issn |
1997-7298
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
98
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
53-6
|
|
pubmed:dateRevised |
2008-3-31
|
|
pubmed:meshHeading |
pubmed-meshheading:9606901-Child,
pubmed-meshheading:9606901-Child, Preschool,
pubmed-meshheading:9606901-DNA Probes,
pubmed-meshheading:9606901-DNA Replication,
pubmed-meshheading:9606901-Female,
pubmed-meshheading:9606901-Genetic Markers,
pubmed-meshheading:9606901-Humans,
pubmed-meshheading:9606901-In Situ Hybridization, Fluorescence,
pubmed-meshheading:9606901-Karyotyping,
pubmed-meshheading:9606901-Male,
pubmed-meshheading:9606901-Pedigree,
pubmed-meshheading:9606901-Rett Syndrome,
pubmed-meshheading:9606901-Sex Chromosome Aberrations,
pubmed-meshheading:9606901-X Chromosome
|
|
pubmed:year |
1998
|
|
pubmed:articleTitle |
[Cytogenetic and molecular genetic diagnostics of Rett syndrome in children].
|
|
pubmed:publicationType |
Journal Article,
Comparative Study,
English Abstract
|
