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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
1981-12-15
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pubmed:abstractText |
The retinal dystrophy gene, rdy, in the rat displays autosomal linkage of 19.0 +/- 1.7 percent with nonagouti, a, and 31.8 +/- 4.1 percent with Svp-1 in linkage group IV. The data are consistent with the linear order rdy--a--Svp-1, but the orientation of this sequence with respect to the centromere is not known. A congenic strain has been developed from some of the testcross animals in which retinal dystrophic and heterozygous control rats of both pink-eyed and black-eyed phenotyped can be distinguished with pigmentation marker genes.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:issn |
0022-1503
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
72
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
294-6
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:7288145-Animals,
pubmed-meshheading:7288145-Chromosome Mapping,
pubmed-meshheading:7288145-Crosses, Genetic,
pubmed-meshheading:7288145-Female,
pubmed-meshheading:7288145-Genes,
pubmed-meshheading:7288145-Genes, Recessive,
pubmed-meshheading:7288145-Male,
pubmed-meshheading:7288145-Pigmentation Disorders,
pubmed-meshheading:7288145-Rats,
pubmed-meshheading:7288145-Retinal Degeneration
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pubmed:articleTitle |
Assignment of retinal dystrophy (rdy) to linkage group IV of the rat.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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