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Searched: Galloway Mowat Syndrome (GAMOS) via the GON7��Gene

Search Results

TNF-Receptor Associated Periodic Syndrome (TRAPS) via the TNFRSF1A Gene

Test Code

Method

Price

8609

Sequencing with CNV PG-Select

$640
Ehlers-Danlos syndrome Musculocontractural Type 1 via the CHST14 Gene

Test Code

Method

Price

12055

Sequencing with CNV PGxome

$890

2507

Sanger Sequencing

$490
Familial Episodic Pain Type 2 Syndrome via the SCN10A Gene

Test Code

Method

Price

11639

Sequencing with CNV PGxome

$890

1795

Sanger Sequencing

$1620
Lesch-Nyhan Syndrome, HPRT-Related Hyperuricemia and Gout via the HPRT1 Gene

Test Code

Method

Price

7129

Sequencing with CNV PG-Select

$640
Leigh Syndrome Associated with Mitochondrial Complex I Deficiency via the NDUFA9 Gene

Test Code

Method

Price

3307

Sanger Sequencing

$910

8207

Sequencing with CNV PGxome

$890
Leigh Syndrome Associated with Mitochondrial Complex I Deficiency via the NDUFS7 Gene

Test Code

Method

Price

3313

Sanger Sequencing

$840

8301

Sequencing with CNV PGxome

$890
Leigh Syndrome Associated with Isolated Complex I Deficiency via the NDUFA12 Gene

Test Code

Method

Price

3309

Sanger Sequencing

$610

8761

Sequencing with CNV PGxome

$890
Liddle Syndrome and Autosomal Recessive Pseudohypoaldosteronism Type 1 via the SCNN1B Gene

Test Code

Method

Price

11649

Sequencing with CNV PGxome

$890

1273

Sanger Sequencing

$870
Leigh Syndrome Associated With Mitochondrial Complex I Deficiency via the NDUFAF2 Gene

Test Code

Method

Price

3310

Sanger Sequencing

$580

10027

Sequencing with CNV PGxome

$890
Leigh Syndrome Associated With Mitochondrial Complex I Deficiency via the NDUFS1 Gene

Test Code

Method

Price

11511

Sequencing with CNV PGxome

$890

2929

Sanger Sequencing

$1190
Liddle Syndrome and Autosomal Recessive Pseudohypoaldosteronism Type 1 via the SCNN1G Gene

Test Code

Method

Price

11651

Sequencing with CNV PGxome

$890

1274

Sanger Sequencing

$780
Hermansky-Pudlak Syndrome Type 9 (HPS9) via the BLOC1S6/PLDN Gene

Test Code

Method

Price

758

Sanger Sequencing

$610

8749

Sequencing with CNV PGxome

$890
Immunodysregulation, Polyendocrinopathy, Enteropathy, X-linked (IPEX) Syndrome via the FOXP3 Gene

Test Code

Method

Price

1838

Sanger Sequencing

$870

8241

Sequencing with CNV PGxome

$890
Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 via the PIGA Gene

Test Code

Method

Price

5761

Sanger Sequencing

$610
Cerebroretinal Microangiopathy with Calcifications and Cysts (Coats plus syndrome) via the CTC1 Gene

Test Code

Method

Price

2007

Sanger Sequencing

$1220

8043

Sequencing with CNV PGxome

$890
Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome via the CALM1 Gene

Test Code

Method

Price

2133

Sanger Sequencing

$650

3963

Sequencing with CNV PGxome

$890
Chondrodysplasia with Joint Dislocations/Catel–Manzke Syndrome via the BPNT2/IMPAD1 Gene

Test Code

Method

Price

2338

Sanger Sequencing

$750

9945

Sequencing with CNV PGxome

$890
Alpha-Thalassemia X-linked Intellectual Disability Syndrome via the ATRX Gene

Test Code

Method

Price

9835

Sequencing with CNV PG-Select

$640
Distal Arthrogryposis Type 7 (Trismus-Pseudocamptodactyly Syndrome) via the MYH8 Gene

Test Code

Method

Price

2282

Sanger Sequencing

$1620

9839

Sequencing with CNV PGxome

$890
Macrocephaly, Alopecia, Cutis Laxa and Scoliosis (MACS) Syndrome via the RIN2 Gene

Test Code

Method

Price

8125

Sequencing with CNV PG-Select

$640

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Search Results

TNF-Receptor Associated Periodic Syndrome (TRAPS) via the TNFRSF1A Gene

Ehlers-Danlos syndrome Musculocontractural Type 1 via the CHST14 Gene

Familial Episodic Pain Type 2 Syndrome via the SCN10A Gene

Lesch-Nyhan Syndrome, HPRT-Related Hyperuricemia and Gout via the HPRT1 Gene

Leigh Syndrome Associated with Mitochondrial Complex I Deficiency via the NDUFA9 Gene

Leigh Syndrome Associated with Mitochondrial Complex I Deficiency via the NDUFS7 Gene

Leigh Syndrome Associated with Isolated Complex I Deficiency via the NDUFA12 Gene

Liddle Syndrome and Autosomal Recessive Pseudohypoaldosteronism Type 1 via the SCNN1B Gene

Leigh Syndrome Associated With Mitochondrial Complex I Deficiency via the NDUFAF2 Gene

Leigh Syndrome Associated With Mitochondrial Complex I Deficiency via the NDUFS1 Gene

Liddle Syndrome and Autosomal Recessive Pseudohypoaldosteronism Type 1 via the SCNN1G Gene

Hermansky-Pudlak Syndrome Type 9 (HPS9) via the BLOC1S6/PLDN Gene

Immunodysregulation, Polyendocrinopathy, Enteropathy, X-linked (IPEX) Syndrome via the FOXP3 Gene

Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 via the PIGA Gene

Cerebroretinal Microangiopathy with Calcifications and Cysts (Coats plus syndrome) via the CTC1 Gene

Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome via the CALM1 Gene

Chondrodysplasia with Joint Dislocations/Catel–Manzke Syndrome via the BPNT2/IMPAD1 Gene

Alpha-Thalassemia X-linked Intellectual Disability Syndrome via the ATRX Gene

Distal Arthrogryposis Type 7 (Trismus-Pseudocamptodactyly Syndrome) via the MYH8 Gene

Macrocephaly, Alopecia, Cutis Laxa and Scoliosis (MACS) Syndrome via the RIN2 Gene