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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1991-7-18
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pubmed:abstractText |
We have used recombinant clones derived from microdissection of the fragile X region to characterize breakpoints around the fragile site at Xq27.3. So far, no microdissection markers derived from Xq28 material have been found, thus allowing a rapid screening for clones surrounding the fragile site by their presence in a somatic cell hybrid containing Xq27.2-Xqter. A total of 43 new DNA markers from Xq27 have been sublocalized within this chromosome band. Of these new DNA markers, 5 lie in an interval defined as containing the fragile X region. The saturation of Xq27 with DNA markers by microdissection demonstrates the power of this technique and provides the resources for generating a complete physical map of the region.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
May
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pubmed:issn |
0888-7543
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
10
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pubmed:owner |
NLM
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pubmed:authorsComplete |
N
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pubmed:pagination |
243-9
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:2045104-Blotting, Southern,
pubmed-meshheading:2045104-Cell Line,
pubmed-meshheading:2045104-Cloning, Molecular,
pubmed-meshheading:2045104-Fragile X Syndrome,
pubmed-meshheading:2045104-Genetic Markers,
pubmed-meshheading:2045104-Humans,
pubmed-meshheading:2045104-Mutation,
pubmed-meshheading:2045104-Polymerase Chain Reaction,
pubmed-meshheading:2045104-X Chromosome
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pubmed:year |
1991
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pubmed:articleTitle |
Linear order of new and established DNA markers around the fragile site at Xq27.3.
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pubmed:affiliation |
Molecular Genetics Group, John Radcliffe Hospital, Headington, Oxford, United Kingdom.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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