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Technical Standards and Guidelines
2008 Edition with upgrades through March 2007
Overview
A1
Purpose of Guidelines
These voluntary standards have been established as an educational resource to assist medical geneticists in providing accurate and reliable diagnostic genetic laboratory testing consistent with currently available technology and procedures in the areas of clinical cytogenetics, biochemical genetics and molecular diagnostics.
A2
Minimal Criteria
These standards establish
minimal criteria
for clinical genetics laboratories. Many laboratories will exceed these minimal standards.
A3
Voluntary Adherence
Adherence to these
Standards and Guidelines
is completely voluntary
and does not necessarily assure a successful outcome. The
Standards and Guidelines should not be considered inclusive of all proper procedures and tests or exclusive of other procedures and tests that are reasonably directed to obtaining the same results.
A4
Acceptable Variations
It is acknowledged that numerous
acceptable variations
exist in genetic testing methodologies. The accuracy and dependability of all procedures should be documented in each laboratory. This should include in-house validation and/or references to appropriate published literature.
A5
Specialized Testing
Specialized testing
, or testing that is limited to one or a few laboratories, requires appropriate and sufficient documentation of effectiveness to justify its use.
A5
Maintenance of Guidelines
These
Standards and Guidelines
will be
reviewed and updated periodically
to assure their timeliness in this rapidly developing field.
Introduction and Authors
Personnel Policies (Section B)
General Policies (Section C)
Shared Methodologies (Section D)
Clinical Cytogenetics (Section E)
Clinical Biochemical Genetics (Section F)
Clinical Molecular Genetics (Section G)
Disease Specific Laboratory Standards and Guidelines
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