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deal of loss in the network, then the ratio will be lower than 1. In other words, the smaller this number, the greater the amount of loss in the network. The ingress node A maintains a record of the last n QoS Operating Points, and it uses these points to create a graph (this is the Dynamic Throughput Graph, or DTG) by interpolation between the set of n QoS operating points. The x-axis of this graph represents the number of bytes sent, and the y-axis of this graph represents the number of bytes received. At the periodic interval used for computing QoS operating points, the DTG is updated by including the latest QoS operating point. Once a certain number of points have been collected, the oldest QoS operating point is dropped whenever a new QoS operating point is added. This provides a sliding window for computing the DTG and ensures that the most recent measurements are used to compute a DTG.

When addressing the six W s in the SHAMPU de ne phase, the emphasis will switch from the whichway and when to the what (design), but all six W s will still require co-ordinated treatment. The process will be more demanding because the design itself will be more uid, perhaps with a range of quite different concepts requiring comparison and choices. It will also be more demanding because the six W issues associated with later stages in the PLC will usually require more effort. For example, life cycle cost and revenue issues, up to and including nal disposal of the product of the project in some cases, are likely to be subject to much greater uncertainty due to more limited clari cation to date. However, this additional effort invested in developing an understanding of whole project life cycle issues will have ongoing bene ts in the later stages of the project, as well as direct immediate bene ts to the project as a whole. Because there is much more scope to change the project design to re ect whole life issues, it is much more important to understand them properly in order to seize the opportunities provided by the earlier initiation of risk management.

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p, m (p) = m(p)

When the composite ampli er is driven by the standard impedance R0 , the noise at the output of each individual ampli er will be kT0 BfAmp gAmp . The part of this noise originating in each ampli er is kT0 B(fAmp 1)gAmp . Half of this goes to the combiner output and half goes to the output termination so the ampli er noise at the combiner output has the same level as the noise from one ampli er. The source noise is divided and ampli ed and recombines coherently at the combiner output along with the signal. Its power at the output is kT0 BgAmp . (The input termination noise combines coherently in the output termination at the same level.) Therefore the total output noise is kT0 BfAmp gAmp , which is fAmp gAmp greater than the input noise to the module. Since the signal is greater by gAmp at the output than at the input, the noise factor for the composite is the same as for the individual ampli ers: fmodule = Sin Nout 1 = fAmp gAmp = fAmp . Sout Nin gAmp (6.13)

Causes. See Etiology Central auditory processing disorder. See Auditory processing disorder Cerebellar hypoplasia, 361, 408 Cerebellum, 23, 97, 126, 360 Cerebral asymmetry, 21 Cerebral palsy, 246, 309, 510 Cerebrovascular disease, 273 Chelation therapy, 80, 278, 279, 280 Chemotherapy, 210, 211, 212 Childhood cancers. See Leukemia, tumors. Child Behavior Checklist, 35 Children s Memory Scale, 6, 29, 80, 198, 229, 265, 294, 323, 350, 369, 379, 439, 454, 467 Chromosomal anomalies, 387 431 See also speci c disorders Clinical Evaluation of Language Fundamentals, Fourth Edition, 5, 28, 79, 198, 229, 350, 439, 467 Clonidine (Catapres), 163, 164, 165, 398 Cocaine, fetal exposure, 361 362, 367 Cochlear implant, 438 Cognition. See Cognitive functioning Cognitive functioning, 1, 5 Angelman syndrome, 405 autism spectrum disorders, 104 childhood cancer, 214 diabetes type 1, 480, 481 Down syndrome, 390 dyslexia/reading disability, 24 epilepsy, 241, 242, 243, 245 fetal alcohol spectrum disorders, 366 367 fragile X, 395 Klinefelter syndrome, 422 lead, 342, 343 low birth weight, 309 312 neuro bromatosis, 435,436 phenylketonuria (PKU), 497 Prader-Willi syndrome, 409, 410 sickle cell disease, 277 speci c language impairment (SLI), 73, 74 Sturge-Weber syndrome, 465 Tourette syndrome, 155,156 traumatic brain injury (TBI), 188 tuberous sclerosis, 449, 450

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