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Searched: 10025

Search Results

Deafness, Autosomal Dominant 25 (DFNA25) via the SLC17A8 Gene

Test Code

Method

Price

2891

Sanger Sequencing

$870

4023

Sequencing with CNV PGxome

$990
Deafness, Autosomal Recessive 25 (DFNB25) via the GRXCR1 Gene

Test Code

Method

Price

2285

Sanger Sequencing

$540

4005

Sequencing with CNV PGxome

$990
Achondroplasia via the FGFR3 Gene, Exon 10

Test Code

Method

Price

425

Sanger Sequencing

$350
Nemaline Myopathy 10 via the LMOD3 Gene

Test Code

Method

Price

11451

Sequencing with CNV PGxome

$990

4426

Sanger Sequencing

$610
Autosomal Recessive Spinocerebellar Ataxia-10 via the ANO10 Gene

Test Code

Method

Price

9911

Sequencing with CNV PGxome

$990

916

Sanger Sequencing

$860
Deafness, Autosomal Dominant 10 (DFNA10) via the EYA4 Gene

Test Code

Method

Price

11311

Sequencing with CNV PGxome

$990

2482

Sanger Sequencing

$1100
Cataract 10, Multiple Types (CTRCT10) via the CRYBA1 Gene

Test Code

Method

Price

11213

Sequencing with CNV PGxome

$990

2902

Sanger Sequencing

$610
Cerebral Cavernous Malformations via the KRIT1/CCM1 Gene, Exon 10

Test Code

Method

Price

125

Sanger Sequencing

$350
Cerebral Cavernous Malformations via the CCM2 Gene, Exons 2-10 Deletion

Test Code

Method

Price

124

Targeted Deletion

$350
Retinitis Pigmentosa 35 (RP35) and Cone-Rod Dystrophy 10 (CORD10) via the SEMA4A Gene

Test Code

Method

Price

11661

Sequencing with CNV PGxome

$990

670

Sanger Sequencing

$940
Deafness, Autosomal Recessive 8 (DFNB8) and Deafness, Autosomal Recessive 10 (DFNB10) via the TMPRSS3 Gene

Test Code

Method

Price

1852

Sanger Sequencing

$870

4271

Sequencing with CNV PGxome

$990
SLC25A13-Related Disorders via the SLC25A13 Gene

Test Code

Method

Price

15293

Sequencing with CNV PG-Select

$990
Carnitine-Acylcarnitine Translocase Deficiency via the SLC25A20 Gene

Test Code

Method

Price

2183

Sanger Sequencing

$710

11859

Sequencing with CNV PGxome

$990
Mitochondrial Phosphate Carrier Deficiency via the SLC25A3 Gene

Test Code

Method

Price

1252

Sanger Sequencing

$710

8485

Sequencing with CNV PGxome

$990
Primary Ciliary Dyskinesia (PCD) via the ODAD4/TTC25 Gene

Test Code

Method

Price

11897

Sequencing with CNV PGxome

$990
Isolated Nonsyndromic Congenital Heart Defects via the NKX2-5 Gene

Test Code

Method

Price

944

Sanger Sequencing

$490

9115

Sequencing with CNV PGxome

$990
Autosomal Dominant Progressive External Ophthalmoplegia and Hypertrophic Cardiomyopathy with Mitochondrial Myopathy via the SLC25A4 Gene

Test Code

Method

Price

1250

Sanger Sequencing

$580

8831

Sequencing with CNV PGxome

$990
Osteopetrosis via the SNX10 Gene

Test Code

Method

Price

1487

Sanger Sequencing

$650

8685

Sequencing with CNV PGxome

$990
Hypercalciuria via the ADCY10 Gene

Test Code

Method

Price

11073

Sequencing with CNV PGxome

$990

2548

Sanger Sequencing

$1620
TARP Syndrome via the RBM10 Gene

Test Code

Method

Price

2475

Sanger Sequencing

$1280

8029

Sequencing with CNV PGxome

$990

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Search Results

Deafness, Autosomal Dominant 25 (DFNA25) via the SLC17A8 Gene

Deafness, Autosomal Recessive 25 (DFNB25) via the GRXCR1 Gene

Achondroplasia via the FGFR3 Gene, Exon 10

Nemaline Myopathy 10 via the LMOD3 Gene

Autosomal Recessive Spinocerebellar Ataxia-10 via the ANO10 Gene

Deafness, Autosomal Dominant 10 (DFNA10) via the EYA4 Gene

Cataract 10, Multiple Types (CTRCT10) via the CRYBA1 Gene

Cerebral Cavernous Malformations via the KRIT1/CCM1 Gene, Exon 10

Cerebral Cavernous Malformations via the CCM2 Gene, Exons 2-10 Deletion

Retinitis Pigmentosa 35 (RP35) and Cone-Rod Dystrophy 10 (CORD10) via the SEMA4A Gene

Deafness, Autosomal Recessive 8 (DFNB8) and Deafness, Autosomal Recessive 10 (DFNB10) via the TMPRSS3 Gene

SLC25A13-Related Disorders via the SLC25A13 Gene

Carnitine-Acylcarnitine Translocase Deficiency via the SLC25A20 Gene

Mitochondrial Phosphate Carrier Deficiency via the SLC25A3 Gene

Primary Ciliary Dyskinesia (PCD) via the ODAD4/TTC25 Gene

Isolated Nonsyndromic Congenital Heart Defects via the NKX2-5 Gene

Autosomal Dominant Progressive External Ophthalmoplegia and Hypertrophic Cardiomyopathy with Mitochondrial Myopathy via the SLC25A4 Gene

Osteopetrosis via the SNX10 Gene

Hypercalciuria via the ADCY10 Gene

TARP Syndrome via the RBM10 Gene