Shortened normal form

Equations 4a and 5a both show that exposure time can be shortened by increasing the beam brightness, or decreasing the spherical aberration Cs. By plotting these equations in normalized form in Figure 1, absolute pixel... 

The H and 13C NMR data for the three metal derivatives were similar. An X-ray crystallographic structure for the gallium derivative (Fig. 6) indicated a shortened Ga—C (carbene) distance of 1.935(6) A, whereas the Ga—C(Me) distances had normal single bond values, 1.994(8) and 1.988(8) A. Thus, the structure may be visualized as being composed of the two canonical forms... 

Grain boundary defects are primarily responsible for the operation of zinc oxide (ZnO) varistors, a shortened form of variable resistor. The varistor behaves like an insulator or poor semiconductor at lower electrical field strengths, but at a critical breakdown voltage the resistance decreases enormously and the material behaves like an electrical conductor (Fig. 3.36). When a varistor is connected in parallel with electrical equipment, negligible power flows through it under normal low... 

Fig. 10. Representative score assignment for heart, (a) Left side of a heart with normal ventricle and atrium, (b) Ventricle slightly small but within normal range (c) Delineation between ventricle and atrium chambers is not clear. An abnormal dark/dense tissue in the ventricle chamber (arrowy, (d) Both ventricle and atrium chambers have blood congestion and are small. An enlarged and translucent outflow tract is observed above the chambers (arron. (e) Small chambers with abnormal orientation and a very short outflow tract (arron. (f) Right side of a normal heart with normal U shaped outflow tract dotted iine). (g) Outflow tract slightly narrowed (arrows), (h) A kink formed in outflow tract dotted tine), (i) Outflow tract very short and narrow with a kink dotted tind). Q) Abnormally shaped and shortened outflow tract dotted tine).

Classical rhizomelic chondrodysplasia punctata (RCDP) patients have a marked shortening of their proximal extremities, calcified stippling of the epiphyses and cataracts in addition to their absent psychomotor development. Patients with a variant form of RCDP have normal bones, but will have cataracts and some degree of mental retardation. Patients with a deficiency of dihydroxyacetone phosphate acyltransferase are clinically indistinguishable from the classical RCDP phenotype. 

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