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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
859
|
pubmed:dateCreated |
1989-2-2
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Dec
|
pubmed:issn |
0028-8446
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
14
|
pubmed:volume |
101
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
833
|
pubmed:dateRevised |
2004-11-17
|
pubmed:meshHeading |
pubmed-meshheading:3205498-Female,
pubmed-meshheading:3205498-Humans,
pubmed-meshheading:3205498-Neuromuscular Diseases,
pubmed-meshheading:3205498-Sex Chromosome Aberrations,
pubmed-meshheading:3205498-Stereotyped Behavior,
pubmed-meshheading:3205498-Syndrome,
pubmed-meshheading:3205498-X Chromosome
|
pubmed:year |
1988
|
pubmed:articleTitle |
Rett syndrome genetic study.
|
pubmed:publicationType |
Letter
|