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2 subtopics

 

  • Linkage Disequilibrium
  • Lod Score

Linkage (Genetics)Follow by RSS 

You've reached a pubget topic page. Below are the latest papers on this topic, with subtopics on the left.

keywords > Genetic Phenomena > Linkage (Genetics)

Latest papers

QTL detection by multi-parent linkage mapping in oil palm (Elaeis guineensis Jacq.).

Fine mapping of a resistance gene to bacterial leaf pustule in soybean.

Genomic microstructure and differential expression of the genes encoding UDP-glucose:sinapate glucosyltransferase (UGT84A9) in oilseed rape (Brassica napus).

Molecular mapping and candidate gene identification of the Rf2 gene for pollen fertility restoration in sorghum [Sorghum bicolor (L.) Moench].

Variance component methods for analysis of complex phenotypes.

Progressive retinal atrophy in Schapendoes dogs: mutation of the newly identified CCDC66 gene.

Linkage and association study of discoidin domain receptor 1 as a novel susceptibility gene for childhood IgA nephropathy.

A Copine family member, Cpne8, is a candidate quantitative trait gene for prion disease incubation time in mouse.

Suggestive evidence on chromosomes 2 and 19 for HTR1A-independent linkage of genes to major depression.

Potentials and limits of pairwise kinship analysis using autosomal short tandem repeat loci.

Quantitative trait loci in the Ogle/TAM O-301 oat mapping population controlling resistance to Puccinia coronata in the field.

Quantitative trait loci for resistance to Pyrenophora tritici-repentis race 1 in a Chinese wheat.

Confirmation and generalization of an alcohol-dependence locus on chromosome 10q.

Mutation and the evolution of recombination.

Familial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase.

Fine mapping of a gene for low-tiller number, Ltn, in japonica rice (Oryza sativa L.) variety Aikawa 1.

Comprehensive genetic and mutation analysis of familial dementia with Lewy bodies linked to 2q35-q36.

A remark on rare variants.

Study of TNFalpha -308G/A and IL6 -174G/C polymorphisms in type 2 diabetes and obesity risk in the Tunisian population.

HER2 codon 655 polymorphism is associated with advanced uterine cervical carcinoma.

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