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Searched: Parkinson Disease Sequencing Panel with CNV Detection
Search Results
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…variants (CNVs). This panel will detect all these variant types. Notably, the vast majority of CNVs, including 16p11.2 deletion syndrome and Smith-Magenis syndrome (17p11.2) will be detected. This panel is not designed to diagnose Prader…
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Test CodeMethodPrice10337Sequencing with CNV PGxome$990
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Test CodeMethodPrice10623Sequencing with CNV PGxome$990
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Test CodeMethodPrice11325Sequencing with CNV PGxome$9903390Sanger Sequencing$810
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Test CodeMethodPrice11457Sequencing with CNV PGxome$990639Sanger Sequencing$2520
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Test CodeMethodPrice13037Sequencing with CNV PGxome$990
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Test CodeMethodPrice1731Sanger Sequencing$9908129Sequencing with CNV PGxome$990
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Test CodeMethodPrice11607Sequencing with CNV PGxome$9901027Sanger Sequencing$840
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Test CodeMethodPrice11703Sequencing with CNV PGxome$990
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Test CodeMethodPrice12609Sequencing with CNV PGxome$990
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…Dr. Diane Allingham-Hawkins, Ph.D, FCCMG, FACM, the Senior Laboratory Director & Dean of Geneticists at PreventionGenetics presents "Getting More From Your Sequencing Test Copy Number Variant Detection by Next Generation Sequencing…
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Test CodeMethodPrice13021Sequencing with CNV PGxome$990
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Test CodeMethodPrice9821Sequencing with CNV PG-Select$990
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Test CodeMethodPrice12607Sequencing with CNV PGxome$990
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Test CodeMethodPrice1029Sanger Sequencing$6508687Sequencing with CNV PGxome$990
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Test CodeMethodPrice11225Sequencing with CNV PGxome$990382Sanger Sequencing$1650
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Test CodeMethodPrice3017Sequencing with CNV PGxome$990
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Test CodeMethodPrice11587Sequencing with CNV PGxome$9901028Sanger Sequencing$780
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…Sclerosis (ALS), Parkinson Disease, Muscular Dystrophy and much more. Accurate genetic testing is imperative for diagnosis, informed treatment decisions and identifying other family members that may be at risk. CMA Amyotrophic Lateral…
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Test CodeMethodPrice11603Sequencing with CNV PGxome$990199Sanger Sequencing$910
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