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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1990-3-9
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pubmed:abstractText |
Employing 16 polymorphic DNA markers as well as the chromosome 19 centromere heteromorphism, we have performed a genetic linkage study in 26 families with myotonic dystrophy. Fourteen of these markers had been assigned previously to one of five different intervals of the 19cen-19q13.2 segment by using somatic cell hybrids. For the long arm of chromosome 19, a genetic map that encompasses 9 polymorphic markers and the DM gene has been constructed. Our studies indicate that the DM and CKMM genes map distal to the ApoC2-ApoE gene cluster and to the anonymous polymorphic markers D19S15 and D19S16, but proximal to the D19S22 marker. The orientation of DM and CKMM remains to be determined.
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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 |
Oct
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pubmed:issn |
0888-7543
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
5
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
589-95
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pubmed:dateRevised |
2010-11-18
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pubmed:meshHeading |
pubmed-meshheading:2575588-Chromosome Mapping,
pubmed-meshheading:2575588-Chromosomes, Human, Pair 19,
pubmed-meshheading:2575588-Crossing Over, Genetic,
pubmed-meshheading:2575588-DNA Mutational Analysis,
pubmed-meshheading:2575588-Female,
pubmed-meshheading:2575588-Genetic Linkage,
pubmed-meshheading:2575588-Genetic Markers,
pubmed-meshheading:2575588-Humans,
pubmed-meshheading:2575588-Male,
pubmed-meshheading:2575588-Muscular Dystrophies,
pubmed-meshheading:2575588-Polymorphism, Restriction Fragment Length,
pubmed-meshheading:2575588-Recombination, Genetic
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pubmed:year |
1989
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pubmed:articleTitle |
A multipoint linkage map around the locus for myotonic dystrophy on chromosome 19.
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pubmed:affiliation |
Department of Human Genetics, University Hospital, 6500HB Nijmegen, The Netherlands.
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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