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Searched: Wolfram Syndrome Sanger Sequencing Panel
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Test CodeMethodPrice10057Sequencing with CNV PGxome$990
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Test CodeMethodPrice1478Sanger Sequencing$44010045Sequencing with CNV PGxome$990
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Test CodeMethodPrice1477Sanger Sequencing$8708265Sequencing with CNV PGxome$990
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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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…Code Method Price 440 Sanger Sequencing $710 9963 Sequencing with CNV PGxome $990 Wolfram Syndrome Panel Test Code Method Price 10057 Sequencing with CNV PGxome $990 Wolfram Syndrome Type 2 via the CISD2 Gene Test Code Method Price 1478…
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…Neoplasia Obesity Pancreatitis Paraganglioma-Pheochromocytoma Syndrome Premature Ovarian Failure (POF) Septo-optic Dysplasia Shwachman-Diamond Syndrome Thyroid Hormone Resistance Von Hippel-Lindau Disease Warburg Micro 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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…Sequencing with CNV PGxome $990 Wolfram Syndrome Panel Test Code Method Price 10057 Sequencing with CNV PGxome $990 Wolfram Syndrome Type 2 via the CISD2 Gene Test Code Method Price 1478 Sanger Sequencing $440 10045 Sequencing with CNV…
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…, Hemiplegia and Migraines Stuttering Tay-Sachs Disease (GM2 Gangliosidosis Type 1) Tuberous Sclerosis Warburg Micro Syndrome Wolfram Syndrome…
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…Panel Test Code Method Price 10447 Sequencing with CNV PGxome $990 Wolfram Syndrome Panel Test Code Method Price 10057 Sequencing with CNV PGxome $990 GO BACK Test By Category View All Tests NY Tests Only ORDER Test Kits START Custom Panel…
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Test CodeMethodPrice4303Sequencing with CNV PGxome$990
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Test CodeMethodPrice10331Sequencing with CNV PGxome$990
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…of HL are also included in this panel (Perrault, Treacher Collins, Stickler, Jervell and Lange-Nielsen, branchio-oto-renal (BOR), Wolfram, Heimler, and Alport syndromes). Copy number variant (CNV) detection is an important component…
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Test CodeMethodPrice2034Sanger Sequencing$6509997Sequencing with CNV PGxome$990
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Test CodeMethodPrice5063Sequencing with CNV PGxome$1290
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Test CodeMethodPrice10305Sequencing with CNV PGxome$990
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Test CodeMethodPrice12001Sequencing with CNV PGxome$1290
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Test CodeMethodPrice12003Sequencing with CNV PGxome$1290
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Test CodeMethodPrice15423Sequencing with CNV PGxome$1390
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Test CodeMethodPrice3257Sequencing with CNV PGxome$990
RESULTS KEY
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