CiteSeerX — Concerns Related to Biochemical Genetic Testing................................5

Concerns Related to Biochemical Genetic Testing................................5

Cached

Download Links

[www.cdc.gov]

by Unknown Authors

BibTeX

@MISC{_concernsrelated,
    author = {},
    title = {Concerns Related to Biochemical Genetic Testing................................5},
    year = {}
}

Bookmark

OpenURL

Abstract

Citations

19	Laboratory Standards Institute, Methods for antimicrobial dilution and disk susceptibility testing of infrequently isolated or fastidious bacteria - Clinical - 2006
10	L: The continuum of translation research in genomic medicine: how can we accelerate the appropriate integration of human genome discoveries into health care and disease prevention. Genetics in Medicine 2007 - MJ, Gwinn, et al.
5	Drug Administration. Guidance for industry and FDA reviewers: content and format of premarket notification [510(k)] submissions for liquid chemical sterilants/high level disinfectants - Food
5	Promoting safe and effective genetic tests in the United States: work of the task force on genetic testing. Clin Chem - NA - 1999
5	privacy rule and public health: guidance from - HIPAA
3	Screening and Genetics Resource Center. National newborn screening report 2000 - Newborn - 2003
3	Laboratory Standards Institute. Application of a quality management system model for laboratory services; approved guideline - Clinical - 2011
3	Proficiency test performance as a predictor of accuracy of routine patient testing for theophylline. Clin Chem - RW, KY - 1993
3	Desnick RJ, Keenlyside R. Quality assurance in molecular genetic testing laboratories. JAMA - MM, MO, et al. - 1999
3	Making the case for objective performance metrics in newborn screening by tandem mass spectrometry. Ment Retard Dev Disabil Res Rev 2006;12:255–61 - Rinaldo, Zafari, et al.
3	et al. Guidelines for the retention, storage, and use of residual dried blood spot samples after newborn screening analysis: statement of the Council of Regional Networks for Genetic Services. Biochem Mol Med - BL, WH, et al. - 1996
3	Laboratory Standards Institute, Interpretive criteria for identification of bacteria and fungi by DNA target sequencing: approved guideline. CLSI document MM18-A - Clinical - 2008
3	Laboratory Standards Institute. Protection of Laboratory Workers From Occupationally Acquired Infections; Approved Guideline M29-A3, 3rd Edition - Clinical
3	Laboratory Standards Institute. Collection, transport, preparation, and storage of specimens for molecular methods; approved guideline - Clinical - 2005
2	Personnel standards and quality assurance practices of biochemical genetic testing laboratories in the United States. Arch Pathol Lab Med 2003;127:71–6 - MM, Benach, et al.
2	Laboratory Improvement Advisory Committee (CLIAC). February 9–10, 2010: meeting summary - Clinical - 2010
2	Cassiman JJ. Evaluation of CFTR gene mutation testing methods in 136 diagnostic laboratories: report of a large European external quality assessment - Dequeker - 1998
2	Laboratory Standards Institute. Assessment of laboratory tests when proficiency testing is not available; approved guideline - Clinical - 2008
2	Improving newborn screening laboratory test ordering and results reporting using health information exchange. J Am Med Inform Assoc 2010;17:13–8 - SM, PC, et al.
2	State Department of Health. Approved laboratories - York - 2012
2	Department of Health. Office of Laboratory Quality Assurance - State
2	Laboratory Standards Institute. Evaluation of the linearity of quantitative measurement procedures; A statistical approach; Approved guideline; Clinical and Laboratory Standards Institute - Clinical - 2003
2	Laboratory Standards Institute. Using proficiency testing to improve the clinical laboratory; approved guideline - Clinical - 2007
2	for Medicare & Medicaid Services. Clinical Laboratory Improvement Amendment (CLIA) proficiency testing: dos and don’ts - Centers
2	State Department of Health. Clinical laboratory evaluation program: survey standards - York - 2012
2	Laboratory Standards Institute. Laboratory documents: development and control; approved guideline - Clinical - 2006
2	Khoury MJ. Evaluation of the validity and utility of genetic testing for rare diseases. Adv Exp Med Biol - SD, Kalman
1	Graf WD. Inborn errors of metabolism in infancy and early childhood: an update. Am Fam Physician 2006;73 - TS, Garg - 1981
1	Newborn screening: toward a uniform screening panel and system. Genet Med 2006;8(Suppl 1):1S–252S - MS, MY, et al.
1	laboratory practices for molecular genetic testing for heritable diseases and conditions - Good
1	Using tandem mass spectrometry for metabolic disease screening among newborns: a report of a work group - CDC
1	et al. National Academy of Clinical Biochemistry laboratory medicine practice guidelines: follow-up testing for metabolic disease identified by expanded newborn screening using tandem mass spectrometry; executive summary. Clin Chem 2009;55:1615–26 - DJ, Rinaldo, et al.
1	for Medicare & Medicaid Services. 42 C.F.R. Part 493. Laboratory Requirements: Clinical Laboratory Improvement Amendments of - Centers - 1988
1	Strovel ET. Management and quality assurance in the biochemical genetics laboratory. Curr Protoc Hum Genet 2008;17.7.1–17.7.12 - TM
1	Achieving and maintaining quality in the laboratory. Haemophilia 2006;12 (Suppl 3):61–7 - MS, Mammen, et al.
1	Garbade SF, Langhans CD, et al. Qualitative urinary organic acid analysis: methodological approaches and performance. J Inherit Metab Dis 2008;31:690–6 - Peters
1	Burlina A, Kozich V, Vianey-Saban C. Quality of analytical performance in inherited metabolic disorders: the role of ERNDIM. J Inherit Metab Dis 2008;31:680–9 - Fowler
1	Reilly AA, Esernio-Jenssen D, et al. Evaluation of blood lead proficiency testing: comparison of open and blind paradigms. Clin Chem 2001;47:322–30 - PJ
1	European Research Network for Evaluation and Improvement of Screening, Diagnosis, and Treatment of Inherited Disorders of Metabolism (ERNDIM). The Eurogentest project and ERNDIM. Interim report on biochemical genetic testing in Europe: deficits and needs - Sheffield - 2012
1	Improving and assuring newborn screening laboratory quality worldwide: 30-year experience at the Centers for disease Control and Prevention. Semin Perinatol 2010;34:125–33 - VR, JV, et al.
1	et al; Newborn Screening Workgroup of the Heartland Regional Genetics and Newborn Screening Collaborative. The heartland good spot/bad spot project - McCallister, Himstedt, et al. - 2010
1	National evaluation of U.S. newborn screening system components. Ment Retard Dev Disabil Res Rev 2006;12:236–45 - BL, WH
1	standardization and quality assurance programs: newborn screening quality assurance program - Laboratory
1	et al. Standardizing newborn screening results for health information exchange - Abhyankar, MA, et al.
1	Informatics Institute. Newborn dried blood spot (NDBS) screening implementation guide for laboratory results - Health - 2012
1	Outcomes from tandem mass spectrometry (MS/MS) workshops in the United States and the performance evaluation of MS/MS laboratories. Southeast Asian J Trop Med Public Health 2003; 34(Suppl 3):121–6 - WH, Lim, et al.
1	Mockridge P. Detection and correction of systematic laboratory problems by analysis of clustered proficiency testing failures. Arch Pathol Lab Med 2005;129:186–9 - GA, MG, et al.
1	Reduction of the false-positive rate in newborn screening by implementation of MS/MS-based second-tier tests: the Mayo Clinic experience (2004– 2007). J Inherit Metab Dis 2007;30:585–92 - Matern, Tortorelli, et al.
1	Clinical biochemical genetics in the twenty-first century. Acta Paediatr Suppl 2004;93:22–6 - Rinaldo, Hahn, et al.
1	Newborn screening of metabolic disorders: recent progress and future developments. Nestle Nutr Workshop Ser Pediatr Program 2008;62:81–93 - Rinaldo, JS, et al.