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have an IHS. The first question in your mind will probably be, Are they powerful enough And the answer is yes, with the exception of the Celeron M. We will set that one aside, and look at the Pentium M, Dothan core, and the Turion 64. Industrial desktop boards for the Pentium M have been around almost as long as the processor itself. AOpen and DFI were the first to introduce consumer-friendly P-M boards in Q4 2004. These were based on the older Intel 855 chipset, which had a few limitations, the biggest being single channel memory. The DFI board was equipped with a small proprietary heat sink whose fan still had to work pretty hard to keep even the P-M cool enough, but the AOpen board featured a socket 478 HS retention bracket that made it possible to use any of a huge range of capable aftermarket heat sinks for super quiet cooling (see Figure 5-7).



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delete a parameter/value pair, highlight it and click the Delete ( ) button at the top of the Parameter column. add a new parameter, click the Add (+) button to move to the first blank line, and use Tab to move to the next parameter. move a parameter from one position in the list to another, highlight it and click the up or down arrow buttons at the top of the Parameter column.

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Expectation models and corresponding reference least squares criteria. (a) Exponentially damped cosine expectation model (solid line) and its values at the measurement points (circles). (b) Contours of corresponding reference nonlinear least squares criterion as a function of the decay constant and frequency with minimum (cross). (c) Gaussian peak expectation model (solid line) and its values at the measurement points (circles). (d) Contours of the correspondingreference nonlinear least squares criterion as a function of the location and half-width of the peak with minimum (cross). The linear parameters, the amplitude of the damped cosine, and the height of the peak have been eliminated from the criterion. (Example 6.6)

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DnB (MHz) nB (GHz) 163.0 69.2 107 72.9 82.3 100.4 219 12.5 165 45.6 253.7 32.6 32 30.5 28.5 19.6 21.0 27.8 26.3 34.6 37.1 15.7

(8.16) (8.17)

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selectivity and speci city are often used interchangeably However, there are debates over the use of speci city over selectivity and some authorities, for example, the International Union of Pure and Applied Chemistry (IUPAC), have preferred the term selectivity, reserving speci city for those procedures that are completely selective For pharmaceutical application, the above de nition of ICH will be used For identity test, compounds of closely related structures which are likely to be present should be discriminated from each other This could be con rmed by obtaining positive results (by comparison with a known reference material) from samples containing the analyte, coupled with negative results from samples which do not contain the analyte Furthermore, the identi cation test may be applied to material structurally similar or closely related to the analyte to con rm that a positive response is not obtained.

If you don t see these results, first select each viewport in turn, making sure that both the VP scale and the annotation scale are the same, and that the left viewport is set to 1:2 and the right viewport is set to 1:1. Also, return to model space, select the dimensions that appear incorrect, right-click them, and choose Annotative Object Scale Add/Delete Scales. In the Annotation Object Scale dialog box, make sure that the scales are correct; if not, add or delete a scale as necessary.

The choice of such potentially interfering materials should be based on sound scienti c judgment with a consideration of the interferences that could occur The speci city for an assay and impurity tests should be approached from two angles: 1 When Impurities Are Available The speci city of an assay method is determined by comparing test results from an analysis of sample containing the impurities, degradation products, or placebo ingredients with those obtained from an analysis of samples without the impurities, degradation products, or placebo ingredients For a stability-indicating assay method, degradation peaks need to be resolved from the drug substance However, these impurities do not need to be resolved from each other.

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