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Searched: 6921

Search Results

Spastic Paraplegia 12 via the RTN2 Gene

Test Code

Method

Price

2853

Sanger Sequencing

$780

4917

Sequencing with CNV PGxome

$990
Neuronal Ceroid Lipofuscinosis 12 via the ATP13A2 Gene

Test Code

Method

Price

11097

Sequencing with CNV PGxome

$990

2107

Sanger Sequencing

$1500
IL-12 Receptor B1 Deficiency via the IL12RB1 Gene

Test Code

Method

Price

1768

Sanger Sequencing

$1220

8045

Sequencing with CNV PGxome

$990
Lissencephaly-6 with Microcephaly via the KATNB1 Gene

Test Code

Method

Price

5421

Sequencing with CNV PGxome

$990
Spastic Paraplegia 6 via the NIPA1 Gene

Test Code

Method

Price

2847

Sanger Sequencing

$610

8801

Sequencing with CNV PGxome

$990
Deafness, X-linked 6 (DFNX6) via the COL4A6 Gene

Test Code

Method

Price

11195

Sequencing with CNV PGxome

$990

994

Sanger Sequencing

$1940
6-Pyruvoyltetrahydropterin Synthase (PTPS) Deficiency via the PTS Gene

Test Code

Method

Price

1868

Sanger Sequencing

$650

11889

Sequencing with CNV PGxome

$990
Deafness, Autosomal Recessive 6 (DFNB6) via the TMIE Gene

Test Code

Method

Price

1479

Sanger Sequencing

$540

4031

Sequencing with CNV PGxome

$990
Glucose-6-Phosphate Dehydrogenase Deficiency via the G6PD Gene

Test Code

Method

Price

7657

Sequencing with CNV PGxome

$990
Type 6 Familial Partial Lipodystrophy via the LIPE Gene

Test Code

Method

Price

13073

Sequencing with CNV PGxome

$990
Oculocutaneous Albinism Type 6 (OCAVI) via the SLC24A5 Gene

Test Code

Method

Price

2284

Sanger Sequencing

$750

4239

Sequencing with CNV PGxome

$990
Achromatopsia 6 or Retinal Cone Dystrophy 3 via the PDE6H Gene

Test Code

Method

Price

2438

Sanger Sequencing

$490

7961

Sequencing with CNV PGxome

$990
Deafness, Autosomal Dominant 12 (DFNA12) and Deafness, Autosomal Recessive 21 (DFNB21) via the TECTA Gene

Test Code

Method

Price

11739

Sequencing with CNV PGxome

$990

2063

Sanger Sequencing

$1560
Charcot-Marie-Tooth Type X-linked Dominant 6 via the PDK3 Gene

Test Code

Method

Price

11565

Sequencing with CNV PGxome

$990

2965

Sanger Sequencing

$870
Test By Disease

…Acute Alcohol Sensitivity 1 Acute Intermittent Porphyria 7 Acute Lymphoblastic Leukemia 10 Adams-Oliver Syndrome 1 12 Adams-Oliver Syndrome 2 12 Adams-Oliver Syndrome 3 6 Adams-Oliver Syndrome 4 10 Adams-Oliver Syndrome 5 8 Adams-Oliver…
'Bull's Eye' Macular Dystrophy (BEM), Cone-Rod Dystrophy 12 (CORD12), Retinitis Pigmentosa 41 (RP41) and Stargardt Disease 4 (STGD4) via the PROM1 Gene

Test Code

Method

Price

11609

Sequencing with CNV PGxome

$990

672

Sanger Sequencing

$1310
Ulnar-Mammary Syndrome via the TBX3 Gene

Test Code

Method

Price

15201

Sequencing with CNV PG-Select

$990
Fanconi Anemia via the FANCD2 Gene

Test Code

Method

Price

11321

Sequencing with CNV PGxome

$990
Usher Syndrome Type 1 via the USH1G Gene

Test Code

Method

Price

649

Sanger Sequencing

$580

8933

Sequencing with CNV PGxome

$990
Liddle Syndrome and Autosomal Recessive Pseudohypoaldosteronism Type 1 via the SCNN1B Gene

Test Code

Method

Price

11649

Sequencing with CNV PGxome

$990

1273

Sanger Sequencing

$870

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Search Results

Spastic Paraplegia 12 via the RTN2 Gene

Neuronal Ceroid Lipofuscinosis 12 via the ATP13A2 Gene

IL-12 Receptor B1 Deficiency via the IL12RB1 Gene

Lissencephaly-6 with Microcephaly via the KATNB1 Gene

Spastic Paraplegia 6 via the NIPA1 Gene

Deafness, X-linked 6 (DFNX6) via the COL4A6 Gene

6-Pyruvoyltetrahydropterin Synthase (PTPS) Deficiency via the PTS Gene

Deafness, Autosomal Recessive 6 (DFNB6) via the TMIE Gene

Glucose-6-Phosphate Dehydrogenase Deficiency via the G6PD Gene

Type 6 Familial Partial Lipodystrophy via the LIPE Gene

Oculocutaneous Albinism Type 6 (OCAVI) via the SLC24A5 Gene

Achromatopsia 6 or Retinal Cone Dystrophy 3 via the PDE6H Gene

Deafness, Autosomal Dominant 12 (DFNA12) and Deafness, Autosomal Recessive 21 (DFNB21) via the TECTA Gene

Charcot-Marie-Tooth Type X-linked Dominant 6 via the PDK3 Gene

Test By Disease

'Bull's Eye' Macular Dystrophy (BEM), Cone-Rod Dystrophy 12 (CORD12), Retinitis Pigmentosa 41 (RP41) and Stargardt Disease 4 (STGD4) via the PROM1 Gene

Ulnar-Mammary Syndrome via the TBX3 Gene

Fanconi Anemia via the FANCD2 Gene

Usher Syndrome Type 1 via the USH1G Gene

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