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Searched: Peroxisomal Disorders Sequencing Panel with CNV Detection
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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 CodeMethodPrice10369Sequencing with CNV PGxome$990
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Test CodeMethodPrice4085Sequencing with CNV PG-Select$990
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…Program Overview No-cost genetic testing for 13 genes associated with peroxisomal biogenesis disorders is being offered for qualifying US-resident patients through a program sponsored by Mirum Pharmaceuticals. The genetic test…
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Test CodeMethodPrice7783Sequencing with CNV PG-Select$990
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Test CodeMethodPrice15279Sequencing with CNV PG-Select$990
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Test CodeMethodPrice15275Sequencing with CNV PG-Select$990
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Test CodeMethodPrice15285Sequencing with CNV PG-Select$990
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Test CodeMethodPrice15281Sequencing with CNV PG-Select$990
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Test CodeMethodPrice7781Sequencing with CNV PG-Select$990
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Test CodeMethodPrice11053Sequencing with CNV PGxome$9902892Sanger Sequencing$1590
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Test CodeMethodPrice11249Sequencing with CNV PGxome$990
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…after further laboratory testing. Mirum sponsored reflex testing will include: Reanalysis of ABCD1 gene at PreventionGenetics for verification Panel testing with whole exome sequencing (WES) will be performed…
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Test CodeMethodPrice15277Sequencing with CNV PG-Select$990
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Test CodeMethodPrice7231Sequencing with CNV PG-Select$990
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Test CodeMethodPrice15283Sequencing with CNV PG-Select$990
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Test CodeMethodPrice7787Sequencing with CNV PG-Select$990
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Test CodeMethodPrice7785Sequencing with CNV PG-Select$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 CodeMethodPrice15273Sequencing with CNV PG-Select$990
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