FILTERS
RESULTS KEY
- Tests & Panels
- Categories
- Newsroom
- Custom panels
- Pages & Documents
- Webinars
Searched: Wolfram Syndrome Sequencing Panel with CNV Detection
Search Results
-
…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…
-
Test CodeMethodPrice10057Sequencing with CNV PGxome$990
-
Test CodeMethodPrice1478Sanger Sequencing$44010045Sequencing with CNV PGxome$990
-
Test CodeMethodPrice1477Sanger Sequencing$8708265Sequencing with CNV PGxome$990
-
…-linked Congenital Neutropenia, via the WAS Gene Test 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…
-
…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…
-
…Test 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…
-
…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…
-
…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…
-
…, Hemiplegia and Migraines Stuttering Tay-Sachs Disease (GM2 Gangliosidosis Type 1) Tuberous Sclerosis Warburg Micro Syndrome Wolfram Syndrome…
-
…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…
-
…10185 Sequencing with CNV PGxome $990 Wilms Tumor 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…
-
Test CodeMethodPrice4303Sequencing with CNV PGxome$990
-
Test CodeMethodPrice10331Sequencing with CNV PGxome$990
-
…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…
-
Test CodeMethodPrice2034Sanger Sequencing$6509997Sequencing with CNV PGxome$990
-
Test CodeMethodPrice5063Sequencing with CNV PGxome$1290
-
Test CodeMethodPrice10305Sequencing with CNV PGxome$990
-
Test CodeMethodPrice12001Sequencing with CNV PGxome$1290
-
Test CodeMethodPrice3257Sequencing with CNV PGxome$990
RESULTS KEY
- Tests & Panels
- Categories
- Newsroom
- Custom panels
- Pages & Documents
- Webinars