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At least two distinct selection events can lead to allelic exclusion.
Though the mechanism by which allelic exclusion occurs is not fully understood.
When the allelic frequencies are 0.5, the disequilibrium is maximal.
This results from the many possible allelic combinations.
The populations and subspecies occur on these allelic combinations in different proportions.
Association studies, e.g., allow direct study of allelic effects.
In theory, each phenotype is based upon the allelic variation within the individual genotype.
If allelic, such non-Mendelian interactions are referred to as paramutation.
K ("naked") is the most dominant of the allelic series which controls feather growth rate.
(2) Existence of a gene in several allelic forms.
The difference in populations could reflect variable coverage by available markers or true allelic heterogeneity.
Genetic drift is a cause of allelic frequency change within populations of a species.
There can be no immigration or emigration in the population, because individuals arriving and leaving directly change allelic frequencies.
Genetic heterogeneity can be classified as either "allelic" or "locus".
An important example is capturing only a portion of the variance due to additive (allelic) genetic effects.
As people moved they have tended to lose haplotypes and in the process lose allelic diversity.
Temozolomide appears to have activity in low-grade oligoastrocytomas with a 1p allelic loss.
Watson syndrome is allelic to NF1, the same gene associated with neurofibromatosis type 1.
It changes in toto from one allelic form into another; there are no smaller components within it that can change.
This new population's allelic frequency is probably different from the original population's, and will change how common certain alleles are in the populations.
The gene is associated with allelic variants.
It is also interesting to note that the allelic mutants bmr12 and bmr18 behave differently, even though they are both in the three-dwarf background.
Whether L91' might paramutate an allelic L91 locus remains to be tested.
This type of HH has been shown to be caused by mono allelic mutations.
Allelic interactions similar to paramutation have since been reported in other organisms, including tomatos, peas, and mice.