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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
3
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pubmed:dateCreated |
2002-6-5
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pubmed:abstractText |
[corrected] To investigate the mutation at the transmembrane domain of fibroblast growth factor receptor 3 (FGFR3) nucleotide 1138 site for identifying the major pathologic mechanism of achondroplasia (ACH) and to evaluate the efficacy of denaturing gradient gel electrophoresis(DGGE) method for screening the point mutations.
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pubmed:language |
chi
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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 |
Jun
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pubmed:issn |
1003-9406
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pubmed:author |
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pubmed:issnType |
Print
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
205-8
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pubmed:dateRevised |
2009-11-19
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pubmed:meshHeading |
pubmed-meshheading:12048679-Achondroplasia,
pubmed-meshheading:12048679-DNA,
pubmed-meshheading:12048679-DNA Mutational Analysis,
pubmed-meshheading:12048679-Female,
pubmed-meshheading:12048679-Humans,
pubmed-meshheading:12048679-Male,
pubmed-meshheading:12048679-Point Mutation,
pubmed-meshheading:12048679-Polymorphism, Restriction Fragment Length,
pubmed-meshheading:12048679-Polymorphism, Single-Stranded Conformational,
pubmed-meshheading:12048679-Protein-Tyrosine Kinases,
pubmed-meshheading:12048679-Receptor, Fibroblast Growth Factor, Type 3,
pubmed-meshheading:12048679-Receptors, Fibroblast Growth Factor
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pubmed:year |
2002
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pubmed:articleTitle |
[Detection of fibroblast growth factor receptor 3 gene mutation at nucleotide 1138 site in congenita achondroplasia patients].
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pubmed:affiliation |
The Department of Pediatrics of Shanghai Ruijin Hospital, Shanghai Second Medical University, Shanghai, 200025 P. R. China. skz12@citiz.net
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pubmed:publicationType |
Journal Article,
English Abstract,
Research Support, Non-U.S. Gov't
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