1  and in multilocus microsatellite genotypes (genets).

2 associated with the outward expansion of the genet.

3 spring) for male genets compared with female genets.

4                                      Hum Mol Genet 13:2493-2503, 2004).

5  the variation in selfing, differences among genets accounted for 16.1% of the variation, and statist

6  growth leads to an expansion in the size of genets and increased fitness because large floral displa

7 erved when considering only sexually derived genets and kinship coefficients were significant up to t

8 l expansion of the genetic individual (i.e., genet), and this should decrease distances gametes and s

9 ndity (number of diploid offspring) for male genets compared with female genets.

10 families in the Vinson population, with some genets having as many as eight putative siblings.

11                                              Genets in these two sub-populations appeared to have dif

12  we report on the formation and structure of genets known as symplasmata produced by Pantoea eucalypt

13 ly rooted lianas and all rooted liana stems (genets plus clones).

14 ve propagation) in which parental genotypes (genets) produce vegetative modules (ramets) that are cap

15 ogenetic relationships, 22 S-alleles from 34 genets randomly taken at three Tennessee sites from a ne

16 of these 10 isolates were ramets of a single genet, suggesting a genetic basis underlying the procliv

17 ich fitness was determined by the success of genets through their male and female sex functions.

18   We exposed multiple ramets of 26 goldenrod genets to nutrient or shade stress and to oviposition by

19                                        Plant genets varied widely for an induced 'hypersensitive' res

20 ngens (Scrophulariaceae), each consisting of genets with unique combinations of homozygous marker gen