FILTERS
RESULTS KEY
- Tests & Panels
- Categories
- Newsroom
- Custom panels
- Pages & Documents
- Webinars
Searched: Ciliopathy 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 CodeMethodPrice10431Sequencing with CNV PGxome$1290
-
Test CodeMethodPrice15165Sequencing with CNV PG-Select$990
-
…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…
-
Test CodeMethodPrice15197Sequencing with CNV PG-Select$990
-
Test CodeMethodPrice11803Sequencing with CNV PGxome$990292Sanger Sequencing$1360
-
Test CodeMethodPrice15235Sequencing with CNV PG-Select$990
-
Test CodeMethodPrice10619Sequencing with CNV PGxome$990
-
…Pulmonology Our high quality pulmonology genetic test menu offers panels for various respiratory disorders and has been designed by our expert PhD team. PreventionGenetics’ genetic test menu includes tests for various pulmonology concerns…
-
Test CodeMethodPrice4601Sequencing with CNV PG-Select$990
-
Test CodeMethodPrice10637Sequencing with CNV PGxome$990
-
…Nephrology Our high quality nephrology genetic test menu offers testing for various nephrology disorders and has been curated by our expert PhD team. PreventionGenetics nephrology genetic test menu includes genetic tests and panels…
-
Test CodeMethodPrice577Sanger Sequencing$6108769Sequencing with CNV PGxome$990
-
Test CodeMethodPrice11385Sequencing with CNV PGxome$990623Sanger Sequencing$1430
-
…Osteogenesis Imperfecta Severe Combined Immunodeficiency Syndactyly Top 99 Genetic Causes of Developmental Delay Wilms Tumor Updated Panels Ciliopathy Hereditary Hearing Loss and Deafness Inborn Errors of Immunity/Primary Immunodeficiency…
-
Test CodeMethodPrice15205Sequencing with CNV PG-Select$990
-
…). NPH clinical features overlap with a group of diseases known as ciliopathies, which includes Meckel-Gruber Syndrome, Joubert Syndrome, Bardet-Biedl Syndrome and Leber Congenital Amaurosis. There are also hereditary types of kidney…
-
Test CodeMethodPrice11025Sequencing with CNV PGxome$990640Sanger Sequencing$1690
-
Test CodeMethodPrice11275Sequencing with CNV PGxome$990
-
Test CodeMethodPrice9007Sequencing with CNV PGxome$9901023Sanger Sequencing$540
RESULTS KEY
- Tests & Panels
- Categories
- Newsroom
- Custom panels
- Pages & Documents
- Webinars