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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8723
|
pubmed:dateCreated |
1990-12-3
|
pubmed:commentsCorrections | |
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
AIM
|
pubmed:status |
MEDLINE
|
pubmed:month |
Nov
|
pubmed:issn |
0140-6736
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
3
|
pubmed:volume |
336
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1131
|
pubmed:dateRevised |
2011-11-17
|
pubmed:meshHeading |
pubmed-meshheading:1978006-Alleles,
pubmed-meshheading:1978006-Female,
pubmed-meshheading:1978006-Fragile X Syndrome,
pubmed-meshheading:1978006-Genetic Counseling,
pubmed-meshheading:1978006-Heterozygote,
pubmed-meshheading:1978006-Humans,
pubmed-meshheading:1978006-Intellectual Disability,
pubmed-meshheading:1978006-Male,
pubmed-meshheading:1978006-Sex Factors
|
pubmed:year |
1990
|
pubmed:articleTitle |
Unusual presentation of fragile X syndrome.
|
pubmed:publicationType |
Letter
|