Source:http://linkedlifedata.com/resource/pubmed/id/15952211
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Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
|
pubmed:dateCreated |
2005-6-29
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Jul
|
pubmed:issn |
1552-4825
|
pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
30
|
pubmed:volume |
136
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
278-81
|
pubmed:dateRevised |
2006-11-15
|
pubmed:meshHeading |
pubmed-meshheading:15952211-Base Sequence,
pubmed-meshheading:15952211-Brazil,
pubmed-meshheading:15952211-DNA,
pubmed-meshheading:15952211-DNA Mutational Analysis,
pubmed-meshheading:15952211-Humans,
pubmed-meshheading:15952211-Mutation,
pubmed-meshheading:15952211-Oxidoreductases Acting on CH-CH Group Donors,
pubmed-meshheading:15952211-Smith-Lemli-Opitz Syndrome
|
pubmed:year |
2005
|
pubmed:articleTitle |
DHCR7 mutations in Brazilian Smith-Lemli-Opitz syndrome patients.
|
pubmed:publicationType |
Letter,
Research Support, Non-U.S. Gov't
|