Source:http://linkedlifedata.com/resource/pubmed/id/20236119
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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
2010-6-23
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Jun
|
pubmed:issn |
1399-0004
|
pubmed:author | |
pubmed:issnType |
Electronic
|
pubmed:volume |
77
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
593-7
|
pubmed:meshHeading |
pubmed-meshheading:20236119-Chromosomes, Human, X,
pubmed-meshheading:20236119-Female,
pubmed-meshheading:20236119-Gene Duplication,
pubmed-meshheading:20236119-Humans,
pubmed-meshheading:20236119-Phenotype,
pubmed-meshheading:20236119-Rett Syndrome,
pubmed-meshheading:20236119-Translocation, Genetic
|
pubmed:year |
2010
|
pubmed:articleTitle |
An unbalanced translocation resulting in a duplication of Xq28 causes a Rett syndrome-like phenotype in a female patient.
|
pubmed:publicationType |
Letter,
Case Reports
|