Biomarkers · Chemical
Prader-WilliAngelman Syndrome DNA Methylation Analysis
- Also listed as
- Prader-Willi/Angelman Syndrome, DNA Methylation Analysis, plasma sodium, na, serum sodium
- LOINC codes
- 41117-3
- Tests that measure Prader-WilliAngelman Syndrome DNA Methylation Analysis
- Quest Diagnostics 1
Tests
Check the catalog code, specimen, method and preparation for every test that measures Prader-WilliAngelman Syndrome DNA Methylation Analysis. Select up to five tests to compare them side by side.
Quest Diagnostics 1 test
Panels that include this biomarker
Prader-Willi/Angelman Syndrome, DNA Methylation Analysis 11369
2 analytes · Blood · Fasting not stated · Turnaround Set up: Wed
Quest Diagnostics catalog pageMethod and collection
- Method
- Capillary Electrophoresis • Polymerase Chain Reaction (PCR)
- Collection
- Whole blood: Normal phlebotomy procedure. Store and ship room temperature immediately. Do not freeze. Physician Attestation of Informed Consent - This germline genetic test requires physician attestation that patient consent has been received. Non-Critical
- Reference notes
- See Laboratory Report
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Quest Diagnostics test catalog
1 test: codes, specimens, methods, preparation and reference intervals.
LOINC 41117-3
Regenstrief Institute codes that identify the same result across labs.
Search ClinicalTrials.gov for Prader-WilliAngelman Syndrome DNA Methylation Analysis
Registered studies that measure Prader-WilliAngelman Syndrome DNA Methylation Analysis, on the U.S. National Library of Medicine registry.
Verify these ranges and sources
We compile this page from named laboratory catalogs, guidelines and studies. Labs calculate reference intervals from the people they test, for one assay method and one population group, so an interval describes that population rather than an optimal target.
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