6 - 12 weeks
CLINICAL CONF OF RESEARCH RESU
Clinical Conf Research Shadow
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DNA is analyzed for the presence of a specific mutation, aberration or variation using an appropriate method; applicable methods include fluorescent dideoxynucleotide sequencing, various SNP-detection methods, and copy number detection using semi-quantitative or quantitative PCR, or blotting.
This assay can be used to detect and/or confirm the presence of a specific mutation, aberration or variation previously detected in the patient or a family member in a research laboratory.
Interpretive report provided.
* Reference ranges may change over time. Please refer to the original patient report when evaluating results.
Physicians must contact the MMGL-MGL laboratory at 734-615-2429 prior to sending samples for new testing. A known positive control sample must also be provided. Collect specimen in a lavender top tube. Send intact whole blood specimen within 24 hours if stored at room temperature or within 5 days if stored refrigerated. Alternatively, send 5-10 mcg of highly purified genomic DNA (at a concentration of > or = 0.05 mg/mL) in a 1 X T.E (pH 7.5-8) buffer. The laboratory only accepts DNA that was extracted or isolated by and in a CLIA-certified laboratory or a laboratory meeting equivalent requirements as determined by the CAP and/or the CMS. DNA specimens must pass MMGL quality control analysis before use. Obtaining informed consent from the patient (or legally authorized representative) and ordering physician prior to testing is MANDATORY for this test. If desired, a UMHS Request and Consent for Genetic Testing form can be obtained from the MMGL Molecular Genetics Laboratory by contacting the MLabs Client Services Center at 800-862-7284 or online at https://mlabs.umich.edu/sites/default/files/2020-01/file/pci-mmgl_infor….