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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
4
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pubmed:dateCreated |
2005-8-8
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pubmed:databankReference |
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pubmed:abstractText |
To screen mutations in the forkhead transcriptional factor 2 gene (FOXL2) in six Chinese families with blepharophimosis, ptosis, and epicanthus inversus syndrome(BPES).
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
|
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1003-9406
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pubmed:author |
|
|
pubmed:issnType |
Print
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pubmed:volume |
22
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
372-5
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pubmed:meshHeading |
pubmed-meshheading:16086270-Amino Acid Sequence,
pubmed-meshheading:16086270-Base Sequence,
pubmed-meshheading:16086270-Blepharophimosis,
pubmed-meshheading:16086270-Blepharoptosis,
pubmed-meshheading:16086270-China,
pubmed-meshheading:16086270-Eyelid Diseases,
pubmed-meshheading:16086270-Family Health,
pubmed-meshheading:16086270-Female,
pubmed-meshheading:16086270-Forkhead Transcription Factors,
pubmed-meshheading:16086270-Humans,
pubmed-meshheading:16086270-Male,
pubmed-meshheading:16086270-Molecular Sequence Data,
pubmed-meshheading:16086270-Mutation,
pubmed-meshheading:16086270-Pedigree,
pubmed-meshheading:16086270-Sequence Alignment
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pubmed:year |
2005
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pubmed:articleTitle |
A novel mutation in the FOXL2 gene in a Chinese family with blepharophimosis, ptosis, and epicanthus inversus syndrome.
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pubmed:affiliation |
Weifang Medical College, Weifang, Shandong, 261042 PR China.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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