| 1. |
Neter, J., Kutner, M. H., Wasserman, W., and Nachtsheim, C. J. (1996) Applied Linear Statistical Models, 4th ed. Homewood, Irwin.
|
| |
| 2. |
Clinical and Laboratory Standards Institute. (2004) Evaluation of Precision Performance of Quantitative Measurement Methods; Approved Guideline—Second Edition. EP5-A2. Villanova, Clinical and Laboratory Standards Institute.
|
| |
| 3. |
Littell, R. C., Milliken, G. A., Stroup, W. W., Wolfinger, R. D., and Schabenberger, O. (2006) SAS for Mixed Models, 2nd ed. Cary, SAS Institute.
|
| |
| 4. |
Satterthwaite, F. E. (1946) An approximate distribution of estimates of variance components. Biometrics
2, 110–114.
|
| |
| 5. |
Clinical and Laboratory Standard Institute. (1999) Statistical Quality Control for Quantitative Measurements: Principles and Definitions; Approved Guideline—Second Edition. C24-A2. Villanova, Clinical and Laboratory Standards Institute.
|
| |
| 6. |
Westgard, J. O., and Klee, G. G. (2006) Quality management. In: Burtis, C. A., Ashwood, E. R., and Bruns, D. E., eds. Tietz Textbook of Clinical Chemistry and Molecular Diagnostics, 4th ed. St. Louis, Elsevier Saunders, pp. 485–532.
|
| |
| 7. |
Parvin, C. A. (1997) Quality-control (QC) performance measures and the QC planning process. Clin. Chem.
43, 602–607.
|
| |
| 8. |
Linnet, K. (1991) Mean and variance rules are more powerful or selective than quality control rules based on individual values.
J. Clin. Chem. Clin. Biochem.
29, 417–424.
|
| |
| 9. |
Parvin, C. A. (1993) New insight into the comparative power of quality-control rules that use control observations within
a single analytical run. Clin. Chem.
39, 440–447.
|
| |
| 10. |
Parvin, C. A., and Gronowski, A. M. (1997) Effect of analytical run length on quality-control (QC) performance and the QC
planning process. Clin. Chem.
43, 2149–2154.
|
| |
| 11. |
Parvin, C. A. (1991) Estimating the performance characteristics of quality-control procedures when error persists until detection.
Clin. Chem.
37, 1720–1724.
|
| |
| 12. |
Clinical and Laboratory Standards Institute. (2000) How to Define and Determine Reference Intervals in the Clinical Laboratory; Approved Guideline—Second Edition. C28-A2. Villanova, Clinical and Laboratory Standards Institute.
|
| |
| 13. |
David, H. A., and Nagaraja, H. N. (2003) Order Statistics, 3rd ed. New York, John Wiley & Sons.
|
| |
| 14. |
Parrish, R. S. (1990) Comparison of quantile estimators in normal sampling. Biometrics
46, 247–257.
|
| |
| 15. |
Harrell, F. E., and Davis, C. E. (1982) A new distribution-free quantile estimator. Biometrika
69, 635–640.
|
| |
| 16. |
Solberg, H. E. (2006) Establishment and use of reference values. In: Burtis, C. A., Ashwood, E. R., and Bruns, D. E. eds.
Tietz Textbook of Clinical Chemistry and Molecular Diagnostics, 4th ed. St. Louis, Elsevier Saunders, pp. 425–448.
|
| |
| 17. |
Beran, R., and Hall, P. (1993) Interpolated nonparametric prediction intervals and confidence intervals. J. Roy. Statist. Soc. B
55, 643–652.
|
| |
| 18. |
Harris, E. K., and Boyd, J. C. (1995) Statistical Bases of Reference Values in Laboratory Medicine. New York, Marcel Dekker.
|
| |
| 19. |
Reed, A. H., Henry, R. J., and Mason, W. B. (1971) Influence of statistical method used on the resulting estimate of normal
range. Clin. Chem.
17, 275–284.
|
| |
| 20. |
Horn, P. S., and Pesce, A. J. (2003) Reference intervals: an update. Clin. Chim. Acta.
334, 5–23.
|
| |
| 21. |
Linnet, K. (1987) Two-stage transformation systems for normalization of reference distributions evaluated. Clin. Chem.
33, 381–386.
|
| |