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The remaining source of the variation is, of course, the environment.
The start OD is far less significant after correction whereas the genotype as source of the variation is as significant as when the uncorrected values are used.
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The source of this variation is the combination of intrinsic and extrinsic factors acting at an individual level.
Understanding the source of this variation is complex, because many processes can contribute to size variation, and the relative importance of various sources can change over ontogeny.
The source of that variation is mutation.
Proliferative heterogeneity within neural progenitor cell populations is well established [39] [41] but the source of this variation is largely unknown.
The source of this variation is unknown.
One likely source of this variation is preparation of the calibration source.
One of the sources of this variation is the between-sample variation during one or subsequent menstrual cycles.
One of the possible sources of this variation is the lack of a consistent mineral preparation procedure.
Parametric modelling always allows for the description of variation in the event- or block specific BOLD-response, when the source (or sources) of variation is known a priori and can be specified numerically as parametric regressor.
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