Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
4
pubmed:dateCreated
1981-12-15
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.
pubmed:grant
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:issn
0022-1503
pubmed:author
pubmed:issnType
Print
pubmed:volume
72
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
294-6
pubmed:dateRevised
2007-11-14
pubmed:meshHeading
pubmed:articleTitle
Assignment of retinal dystrophy (rdy) to linkage group IV of the rat.
pubmed:publicationType
Journal Article, Research Support, U.S. Gov't, P.H.S.