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Searched: Usher Syndrome Sequencing Panel
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Test CodeMethodPrice10053Sequencing with CNV PGxome$990
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Test CodeMethodPrice649Sanger Sequencing$5808933Sequencing with CNV PGxome$990
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Test CodeMethodPrice7605Sequencing with CNV PG-Select$990
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Test CodeMethodPrice3059Sequencing with CNV PG-Select$990
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Test CodeMethodPrice11075Sequencing with CNV PGxome$990698Sanger Sequencing$4070
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…Code Method Price 2025 Sanger Sequencing $1100 8083 Sequencing with CNV PGxome $990 Usher Syndrome Panel Test Code Method Price 10053 Sequencing with CNV PGxome $990 Usher Syndrome Type 1 and Deafness, Autosomal Recessive 12 (DFNB12) via…
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Test CodeMethodPrice3225Sequencing with CNV PG-Select$990
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Test CodeMethodPrice3177Sequencing with CNV PG-Select$990
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Test CodeMethodPrice3091Sequencing with CNV PG-Select$990
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Test CodeMethodPrice4879Sequencing with CNV PG-Select$990
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…Code Method Price 2025 Sanger Sequencing $1100 8083 Sequencing with CNV PGxome $990 Usher Syndrome Panel Test Code Method Price 10053 Sequencing with CNV PGxome $990 Usher Syndrome Type 1 via the USH1G Gene Test Code Method Price 649 Sanger…
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Test CodeMethodPrice11807Sequencing with CNV PGxome$990697Sanger Sequencing$870
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Test CodeMethodPrice11567Sequencing with CNV PGxome$9901466Sanger Sequencing$1060
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Test CodeMethodPrice127Sanger Sequencing$7103991Sequencing with CNV PGxome$990
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Test CodeMethodPrice5063Sequencing with CNV PGxome$1290
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…, with the remaining 20% syndromic. Some forms of SHL, called NSHL mimics, have additional associated clinical features that present later in life. For example, Usher syndrome type 1 first presents as congenital profound hearing loss…
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Test CodeMethodPrice4379Sequencing with CNV PGxome$1790
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…in diagnosis and a better understanding of treatment opportunities and management. CMA Alport Syndrome Branchiootorenal Syndrome Hearing Loss Pendred Syndrome Stickler Syndrome Townes-Brocks Syndrome Usher Syndrome Waardenburg Syndrome Wolfram Syndrome…
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…test menu that offers genetic tests and panels for various vision concerns, including, but not limited to cataracts, glaucoma, cone-rod dystrophy and more. CMA Achromatopsia Albinism Alport Syndrome Anophthalmia Anterior Segment Dysgenesis…
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Test CodeMethodPrice12005Sequencing with CNV PGxome$1790
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