Body mass and bone length are complex polygenic traits determined by dozens, if not hundreds of additive genetic loci [ 58- 62].
In budding yeast, systematic genome-wide screens have identified approximately 300 gene products that affect telomere length homeostasis, showing that telomere length control is complex and regulated by numerous processes and pathways (Askree et al, 2004; Gatbonton et al, 2006; Shachar et al, 2008).
Recent analyses and new fossil discoveries suggest that the evolution of hominin limb length proportions is complex, with evolutionary reversals and a decoupling of proportions within and between limbs.
While brief in length, "Uncle Rudolf" is complex in subject matter and structure.
Leukocyte telomere length is a complex trait which is regulated by genetic [3] [6] and environmental factors, such as smoking [7], and it has been associated with many disease phenotypes, such as cardiovascular diseases and diabetes [8] [10].
Measuring birth length is a complex task, and some misclassification errors can be assumed.
Furthermore, design a predictor for B-cell epitopes, which have high variable epitope length, is more complex than predictor for T-cell epitopes [ 14].
However, we emphasize that the relationship between microsatellite mutability and repeat length is more complex than simply the influence of repeat number on the probability of strand slippage (Eckert et al. 2002; Kelkar et al. 2008; Eckert and Hile 2009).
If not all the beats are the same length, the time signature is complex.
However, since the lithology of actual rock strata is complex, the length of IP relaxation process changes greatly.
