| Fabry Disease via the GLA Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Facioscapulohumeral Muscular Dystrophy 2 via the SMCHD1 Gene |
Sanger Sequencing |
$2170 |
Sequencing with CNV
PGxome |
$890 |
|
| Factor V Deficiency via the F5 Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Factor VII Deficiency via the F7 Gene |
Sanger Sequencing |
$750 |
Sequencing with CNV
PGxome |
$890 |
|
| Factor X Deficiency via the F10 Gene |
Sanger Sequencing |
$710 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Adenomatous Polyposis (FAP) via the APC Gene |
Sequencing with CNV
PG-Select |
$540 |
|
| Familial Amyloidosis (Finnish Type) via the GSN Gene |
Sanger Sequencing |
$1020 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Amyloidosis (hATTR) via the TTR Gene |
Sanger Sequencing |
$540 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Amyloidosis via the APOA1 Gene |
Sanger Sequencing |
$580 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Cold Autoinflammatory Syndrome 2 via the NLRP12 Gene |
Sanger Sequencing |
$1020 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Dysautonomia via the ELP1/IKBKAP Gene - Full Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Familial Dysautonomia via the ELP1/IKBKAP Gene - Targeted Variants Analysis |
|
| Familial Episodic Pain Type 2 Syndrome via the SCN10A Gene |
Sanger Sequencing |
$1620 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Episodic Pain Type 3 (FEPS3) Syndrome, Hereditary Sensory and Autonomic Neuropathy Type VII (HSAN7), and other Pain-Related Disorders via the SCN11A Gene |
Sanger Sequencing |
$1620 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Exudative Vitreoretinopathy 1 (FEVR1) via the FZD4 Gene |
Sanger Sequencing |
$580 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Exudative Vitreoretinopathy 5 (FEVR5) via the TSPAN12 Gene |
Sanger Sequencing |
$680 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Exudative Vitreoretinopathy and Retinitis Pigmentosa via the ZNF408 Gene |
Sanger Sequencing |
$780 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Exudative Vitreoretinopathy via the RCBTB1 Gene |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Focal Epilepsy with Variable Foci via the DEPDC5 Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Familial Gastrointestinal Stromal Tumors (GISTs) via the PDGFRA Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Familial Hemiplegic Migraine 1 (FHM1) via the CACNA1A Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Familial Hemiplegic Migraine 2 (FHM2) via the ATP1A2 Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Familial Hemophagocytic Lymphohistiocytosis, X-linked Lymphoproliferative Disease via the SH2D1A Gene |
Sanger Sequencing |
$490 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Hemophagocytic Lymphohistiocytosis, X-linked Lymphoproliferative Disease via the XIAP/BIRC4 Gene |
Sanger Sequencing |
$650 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Hemophagocytic Lymphohistiocytosis-Type 2 (FHL2) via the PRF1 Gene |
Sanger Sequencing |
$590 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Hemophagocytic Lymphohistiocytosis-Type 3 (FHL3) via the UNC13D Gene |
Sanger Sequencing |
$1540 |
Sequencing with CNV
PGxome |
$1140 |
|
| Familial Hemophagocytic Lymphohistiocytosis-Type 3 (FHL3) via the UNC13D Inversion |
|
| Familial Hemophagocytic Lymphohistiocytosis-Type 4 (FHL4) via the STX11 Gene |
Sanger Sequencing |
$480 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Hemophagocytic Lymphohistiocytosis-Type 5 (FHL5) via the STXBP2 Gene |
Sanger Sequencing |
$960 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Hypercholesterolemia and Hypobetalipoproteinemia via the APOB Gene |
Sanger Sequencing |
$1340 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Hypercholesterolemia via the LDLR Gene |
Sanger Sequencing |
$1060 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Hypercholesterolemia via the LDLRAP1 Gene |
Sanger Sequencing |
$780 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Hypercholesterolemia via the PCSK9 Gene |
Sanger Sequencing |
$940 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Hypocalciuric Hypercalcemia (FHH) via the AP2S1 Gene |
Sanger Sequencing |
$650 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Isolated Hypoparathyroidism via the GCM2 Gene |
Sanger Sequencing |
$750 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Isolated Hypoparathyroidism via the PTH Gene |
Sanger Sequencing |
$370 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Isolated Pituitary Adenoma via the AIP Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Familial Limb Girdle Myasthenia Syndrome via the DOK7 Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Familial Limb Girdle Myasthenic Syndrome via the AGRN Gene |
Sanger Sequencing |
$1750 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Limb Girdle Myasthenic Syndrome With Tubular Aggregates via the DPAGT1 Gene |
Sanger Sequencing |
$750 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Lipoprotein Lipase Deficiency via the LPL Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Familial Mediterranean Fever (Renal Amyloidosis) via the MEFV Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Familial Meningioma via the SMARCE1 Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Familial Pityriasis Rubra Pilaris (PRP) via the CARD14 Gene |
Sanger Sequencing |
$1160 |
Sequencing with CNV
PGxome |
$890 |
|
| Familial Platelet Function Disorder via the GP6 Gene |
Sanger Sequencing |
$810 |
Sequencing with CNV
PGxome |
$890 |
|
| Fanconi Anemia via the BRCA2/FANCD1 Gene |
Sequencing with CNV
PG-Select |
$540 |
|
| Fanconi Anemia via the BRIP1/FANCJ Gene |
Sequencing with CNV
PG-Select |
$540 |
|
| Fanconi Anemia via the FANCA Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Fanconi Anemia via the FANCB Gene |
Sanger Sequencing |
$890 |
Sequencing with CNV
PGxome |
$890 |
|
| Fanconi Anemia via the FANCC Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Fanconi Anemia via the FANCD2 Gene |
Sanger Sequencing |
$1930 |
Sequencing with CNV
PGxome |
$1240 |
|
| Fanconi Anemia via the FANCE Gene |
Sanger Sequencing |
$724 |
Sequencing with CNV
PGxome |
$890 |
|
| Fanconi Anemia via the FANCF Gene |
Sanger Sequencing |
$490 |
Sequencing with CNV
PGxome |
$890 |
|
| Fanconi Anemia via the FANCG Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Fanconi Anemia via the FANCI Gene |
Sanger Sequencing |
$1610 |
Sequencing with CNV
PGxome |
$890 |
|
| Fanconi Anemia via the FANCL Gene |
Sanger Sequencing |
$910 |
Sequencing with CNV
PGxome |
$890 |
|
| Fanconi Anemia via the FANCM Gene |
Sanger Sequencing |
$1490 |
Sequencing with CNV
PGxome |
$890 |
|
| Fanconi Anemia via the PALB2/FANCN Gene |
Sequencing with CNV
PG-Select |
$540 |
|
| Fanconi Anemia via the RAD51/FANCR Gene |
Sequencing with CNV
PGxome |
$890 |
|
| Fanconi Anemia via the RAD51C/FANCO Gene |
Sequencing with CNV
PG-Select |
$540 |
|
| Fanconi Anemia via the RFWD3 Gene |
Sequencing with CNV
PGxome |
$890 |
|
| Fanconi Anemia via the SLX4/FANCP Gene |
Sanger Sequencing |
$1120 |
Sequencing with CNV
PGxome |
$890 |
|
| Fanconi-Bickel Syndrome via the SLC2A2 Gene |
Sanger Sequencing |
$750 |
Sequencing with CNV
PGxome |
$890 |
|
| Farber Lipogranulomatosis via the ASAH1 Gene |
Sanger Sequencing |
$840 |
Sequencing with CNV
PGxome |
$890 |
|
| Feingold Syndrome 1 via the MYCN Gene |
Sanger Sequencing |
$650 |
Sequencing with CNV
PGxome |
$890 |
|
| Fetal Akinesia Deformation Sequence 4 via the NUP88 Gene |
Sequencing with CNV
PGxome |
$890 |
|
| FHL1-Myopathies via the FHL1 Gene |
Sanger Sequencing |
$680 |
Sequencing with CNV
PGxome |
$890 |
|
| Fibrodysplasia Ossificans progressiva (FOP) via the ACVR1 Gene |
Sanger Sequencing |
$840 |
Sequencing with CNV
PGxome |
$890 |
|
| Fish-Eye Disease and Norum Disease via the LCAT Gene |
Sanger Sequencing |
$650 |
Sequencing with CNV
PGxome |
$890 |
|
| Floating-Harbor Syndrome via the SRCAP Gene |
Sanger Sequencing |
$2080 |
Sequencing with CNV
PGxome |
$890 |
|
| Focal Dermal Hypoplasia (FDH) via the PORCN Gene |
Sanger Sequencing |
$870 |
Sequencing with CNV
PGxome |
$890 |
|
| Focal Epilepsy with Speech Disorder via the GRIN2A Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Focal Segmental Glomerulosclerosis (FSGS) via the ACTN4 Gene |
Sanger Sequencing |
$1130 |
Sequencing with CNV
PGxome |
$890 |
|
| Focal Segmental Glomerulosclerosis (FSGS) via the ANLN Gene |
Sanger Sequencing |
$1380 |
Sequencing with CNV
PGxome |
$890 |
|
| Focal Segmental Glomerulosclerosis (FSGS) via the CD2AP Gene |
Sanger Sequencing |
$1190 |
Sequencing with CNV
PGxome |
$890 |
|
| FOXC1-Related Disorders via the FOXC1 Gene |
|
| Fragile X Syndrome via FMR1 CGG Repeat Expansion |
Repeat-Primed PCR & MS-PCR |
$390 |
|
| French-Canadian type of Leigh syndrome via the LRPPRC Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Frontonasal Dysplasia (Frontorhiny) via the ALX3 Gene |
Sanger Sequencing |
$610 |
Sequencing with CNV
PGxome |
$890 |
|
| Frontotemporal Dementia via the GRN Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Frontotemporal Dementia via the MAPT Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Fructose-1,6-Bisphosphatase Deficiency via the FBP1 Gene |
Sanger Sequencing |
$610 |
Sequencing with CNV
PGxome |
$890 |
|
| FTO-Deficiency Syndrome via the FTO Gene |
Sequencing with CNV
PG-Select |
$640 |
|
| Fucosidosis via the FUCA1 Gene |
Sanger Sequencing |
$840 |
Sequencing with CNV
PGxome |
$890 |
|
| Fukuyama Congenital Muscular Dystrophy via the FKTN Japanese Founder Mutation |
|
| Fundus Albipunctatus With or Without Cone Dystrophy via the RDH5 Gene |
Sanger Sequencing |
$610 |
Sequencing with CNV
PGxome |
$890 |
|
ORDER