TARP Syndrome via the RBM10 Gene |
Sanger Sequencing |
$1280 |
Sequencing with CNV PGxome |
$890 |
|
Tay-Sachs Disease via the French Canadian Deletion in the HEXA Gene |
|
Tay-Sachs Disease via the HEXA Gene |
Sequencing with CNV PG-Select |
$640 |
|
Telethoninopathy via the TCAP Gene |
Sanger Sequencing |
$440 |
Sequencing with CNV PGxome |
$890 |
|
Temple-Baraitser Syndrome and Zimmermann-Laband Syndrome via the KCNH1 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Temtamy Syndrome via the C12orf57 Gene |
Sequencing with CNV PGxome |
$890 |
|
Tenorio Syndrome via the RNF125 Gene |
Sanger Sequencing |
$710 |
Sequencing with CNV PGxome |
$890 |
|
Thanatophoric Dysplasia (TD) via the FGFR3 Gene |
|
Thiamine Responsive Megaloblastic Anemia via the SLC19A2 Gene |
Sanger Sequencing |
$650 |
Sequencing with CNV PGxome |
$890 |
|
Thoracic Aortic Aneurysm and Dissection (TAAD) via the ACTA2 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Thoracic Aortic Aneurysm and Dissection (TAAD) via the LOX Gene |
Sequencing with CNV PG-Select |
$640 |
|
Thoracic Aortic Aneurysm and Dissection (TAAD) via the MYH11 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Thoracic Aortic Aneurysm and Dissection (TAAD) via the MYLK Gene |
Sequencing with CNV PG-Select |
$640 |
|
Thoracic Aortic Aneurysm and Dissection (TAAD) via the PRKG1 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Thrombocytopenia 2 and Predisposition to Myeloid Malignancies via the ANKRD26 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Thrombocytopenia 4 via the CYCS Gene |
Sanger Sequencing |
$370 |
Sequencing with CNV PGxome |
$890 |
|
Thrombocytopenia 5 and Predisposition for Hematologic Malignancy via the ETV6 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Thrombocytopenia Absent Radius (TAR) Syndrome via the RBM8A 1q21.1 Deletion |
|
Thrombocytopenia Absent Radius (TAR) Syndrome via the RBM8A Gene |
|
Thrombocytopenia Absent Radius (TAR) Syndrome via the RBM8A Gene - Sequencing and 1q21.1 Deletion |
|
Thrombocytopenia and Bleeding Disorder, Platelet Type 19 via the PRKACG Gene |
Sequencing with CNV PGxome |
$890 |
|
Thrombocytopenia and Related Hematopoietic Disorders via the GATA1 Gene |
Sanger Sequencing |
$560 |
Sequencing with CNV PGxome |
$890 |
|
Thrombocytopenia via the GFI1B Gene |
Sanger Sequencing |
$810 |
Sequencing with CNV PGxome |
$890 |
|
Thrombocytopenia via the MASTL Gene |
Sanger Sequencing |
$890 |
Sequencing with CNV PGxome |
$890 |
|
Thrombocytopenia via the PTPRJ Gene |
Sequencing with CNV PGxome |
$890 |
|
Thrombocytopenia with Predisposition to Acute Myelogenous Leukemia via the RUNX1 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Thrombotic Thrombocytopenic Purpura (TTP) via the ADAMTS13 Gene |
Sanger Sequencing |
$1220 |
Sequencing with CNV PGxome |
$890 |
|
Thromboxane A2 Receptor Deficiency via the TBXA2R Gene |
Sanger Sequencing |
$580 |
Sequencing with CNV PGxome |
$890 |
|
Thyroid Hormone Resistance via the THRB Gene |
Sequencing with CNV PG-Select |
$640 |
|
Timothy Syndrome and Brugada Syndrome via the CACNA1C Gene |
Sanger Sequencing |
$2110 |
Sequencing with CNV PGxome |
$890 |
|
TNF-Receptor Associated Periodic Syndrome (TRAPS) via the TNFRSF1A Gene |
Sequencing with CNV PG-Select |
$640 |
|
Tooth Agenesis via the PAX9 Gene |
Sanger Sequencing |
$610 |
Sequencing with CNV PGxome |
$890 |
|
Townes-Brocks Syndrome via the SALL1 Gene |
Sanger Sequencing |
$890 |
Sequencing with CNV PGxome |
$890 |
|
Transcobalamin II Deficiency via the TCN2 Gene |
Sanger Sequencing |
$940 |
Sequencing with CNV PGxome |
$890 |
|
Treacher Collins Syndrome via the POLR1C Gene |
Sanger Sequencing |
$710 |
Sequencing with CNV PGxome |
$890 |
|
Treacher Collins Syndrome via the POLR1D Gene |
Sanger Sequencing |
$440 |
Sequencing with CNV PGxome |
$890 |
|
Treacher Collins Syndrome via the TCOF1 Gene |
Sanger Sequencing |
$1310 |
Sequencing with CNV PGxome |
$890 |
|
TREM2-Related Disorders via the TREM2 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Tricho-Rhino-Phalangeal Syndrome Types I & III via the TRPS1 Gene |
Sanger Sequencing |
$860 |
Sequencing with CNV PGxome |
$890 |
|
Trimethylaminuria via the FMO3 Gene |
Sanger Sequencing |
$710 |
Sequencing with CNV PGxome |
$890 |
|
Triosephosphate Isomerase Deficiency via the TPI1 Gene |
Sanger Sequencing |
$680 |
Sequencing with CNV PGxome |
$890 |
|
Tropomyosin 2-Related Disorders via the TPM2 Gene |
Sanger Sequencing |
$610 |
Sequencing with CNV PGxome |
$890 |
|
Tuberous Sclerosis Complex (TSC) Deletion/Duplication Testing via MLPA |
|
Tuberous Sclerosis Complex via the TSC1 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Tuberous Sclerosis Complex via the TSC2 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Tubular Aggregate Myopathy via the STIM1 Gene |
Sanger Sequencing |
$840 |
Sequencing with CNV PGxome |
$890 |
|
Tumor Predisposition Syndrome, Uveal Melanoma and Mesothelioma via the BAP1 Gene |
Sequencing with CNV PG-Select |
$640 |
|
TYK2 Deficiency via the TYK2 Gene |
Sequencing with CNV PGxome |
$890 |
|
Type 6 Familial Partial Lipodystrophy via the LIPE Gene |
Sequencing with CNV PGxome |
$890 |
|
Type IV Voltage-Gated Sodium Channel (Alpha Subunit)-Related Disorders via the SCN4A Gene |
Sanger Sequencing |
$1340 |
Sequencing with CNV PGxome |
$890 |
|
Type VI Collagenopathy via the COL6A1 Gene |
Sanger Sequencing |
$1440 |
Sequencing with CNV PGxome |
$890 |
|
Type VI Collagenopathy via the COL6A2 Gene |
Sanger Sequencing |
$1230 |
Sequencing with CNV PGxome |
$890 |
|
Type VI Collagenopathy via the COL6A3 Gene |
Sanger Sequencing |
$2110 |
Sequencing with CNV PGxome |
$890 |
|
Type VI-Related Collagenopathy via the COL12A1 Gene |
Sequencing with CNV PG-Select |
$640 |
|
Tyrosinemia Type III and Hawkinsinuria via the HPD Gene |
Sanger Sequencing |
$750 |
Sequencing with CNV PGxome |
$890 |
|
Tyrosinemia, Type I via the FAH Gene |
Sanger Sequencing |
$580 |
Sequencing with CNV PGxome |
$890 |
|
Tyrosinemia, Type II via the TAT Gene |
Sanger Sequencing |
$780 |
Sequencing with CNV PGxome |
$890 |
|