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1 ium and lead levels were determined by flame atomic absorption spectrophotometry.
2 lysis of arsenic content by graphite furnace atomic absorption spectrophotometry.
3 Lens sodium content was measured by atomic absorption spectrophotometry.
4 Blood lead determinations were made by atomic absorption spectrophotometry.
5 lead levels were measured by electrothermal atomic absorption spectrophotometry.
6 nd iron in plasma and CSF were determined by atomic absorption spectrophotometry.
7 rent methods and zinc recoveries compared by atomic absorption spectrophotometry.
8 vity, and lens ion content was determined by atomic absorption spectrophotometry.
9 dium and potassium content was determined by atomic absorption spectrophotometry.
10 Tissue iron levels were measured by atomic absorption spectrophotometry.
11 availability (Ca, Fe and Zn), quantified by atomic absorption spectrophotometry (AAS), and formula v
12 zinc atom as determined by graphite furnace-atomic absorption spectrophotometry and inductively coup
13 improved the processing of erythrocytes for atomic absorption spectrophotometry and mass spectrometr
14 cytes for measurement of Zn concentration by atomic absorption spectrophotometry and stable isotope e
15 g of both, metal ions contents determined by atomic absorption spectrophotometry, and the MIR spectra
16 h curves from a packed microcolumn and flame atomic absorption spectrophotometry (FAAS) detection.
17 es, the solutions were analyzed by flameless atomic absorption spectrophotometry for mercury and silv
19 ular dichroism spectroscopy, iron-binding by atomic absorption spectrophotometry, oligomerization in
21 stology, autofluorescence spectral analysis, atomic absorption spectrophotometry, Perls' iron stain,
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