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Searched: 4211

Search Results

Deafness, Autosomal Recessive 42 (DFNB42) via the ILDR1 Gene

Test Code

Method

Price

11395

Sequencing with CNV PGxome

$990

1849

Sanger Sequencing

$810
Congenital Adrenal Hyperplasia (CAH) due to 11-β-Hydroxylase Deficiency (11-OHD) via the CYP11B1 Gene

Test Code

Method

Price

1268

Sanger Sequencing

$870
Holoprosencephaly-11 via the CDON Gene

Test Code

Method

Price

11167

Sequencing with CNV PGxome

$990

589

Sanger Sequencing

$1270
Cataract Type 11 via the PITX3 Gene

Test Code

Method

Price

2117

Sanger Sequencing

$580

8847

Sequencing with CNV PGxome

$990
Spastic Paraplegia 11 via the SPG11 Gene

Test Code

Method

Price

15299

Sequencing with CNV PG-Select

$990
Lethal Congenital Contracture Arthrogryposis 11 via the GLDN Gene

Test Code

Method

Price

12657

Sequencing with CNV PGxome

$990
Krabbe Disease via the GALC Exons 11-17 (502T/Del)

Test Code

Method

Price

632

Targeted Deletion

$350
Primary Microcephaly, Autosomal Recessive, via the WDR62 Gene

Test Code

Method

Price

293

Sanger Sequencing

$1430

8019

Sequencing with CNV PGxome

$990
Nephronophthisis / Senior-Loken Syndrome and Bardet-Biedl Syndrome via the SDCCAG8 Gene

Test Code

Method

Price

15197

Sequencing with CNV PG-Select

$990
Smith-Magenis and Potocki-Lupski syndromes via the RAI1 Gene

Test Code

Method

Price

15195

Sequencing with CNV PG-Select

$990
Autosomal Dominant Retinitis Pigmentosa 17 (RP17) via the CA4 Gene

Test Code

Method

Price

8521

Sequencing with CNV PGxome

$990

675

Sanger Sequencing

$680
Late-Onset Autosomal Dominant Retinitis Pigmentosa 42 (RP42) and Crisponi/Cold-Induced Sweating Syndrome Type 1(CISS1)-Like Phenotype Associated with Early-Onset Autosomal Recessive Retinitis Pigmentosa via the KLHL7 Gene

Test Code

Method

Price

10499

Sequencing with CNV PGxome

$990
Retinitis Pigmentosa via the IMPDH1 Gene

Test Code

Method

Price

664

Sanger Sequencing

$910

8221

Sequencing with CNV PGxome

$990
RLBP1-Related Disorders via the RLBP1 Gene

Test Code

Method

Price

8695

Sequencing with CNV PGxome

$990

673

Sanger Sequencing

$650
X-Linked Spondyloepiphyseal Dysplasia Tarda (SEDT) via the TRAPPC2 Gene

Test Code

Method

Price

10037

Sequencing with CNV PGxome

$990

819

Sanger Sequencing

$520
Leber Congenital Amaurosis via the CRX Gene

Test Code

Method

Price

9119

Sequencing with CNV PGxome

$990

665

Sanger Sequencing

$490
Isolated Nonsyndromic Congenital Heart Defects via the NKX2-5 Gene

Test Code

Method

Price

944

Sanger Sequencing

$490

9115

Sequencing with CNV PGxome

$990
Myofibrillar Myopathy via the LDB3 (ZASP) Gene

Test Code

Method

Price

11447

Sequencing with CNV PGxome

$990

365

Sanger Sequencing

$940
Hereditary Spherocytosis via the EPB42 Gene

Test Code

Method

Price

11291

Sequencing with CNV PGxome

$990

2122

Sanger Sequencing

$870
Medium Chain Acyl-CoA Dehydrogenase Deficiency via the ACADM Gene

Test Code

Method

Price

180

Sanger Sequencing

$750

9505

Sequencing with CNV PGxome

$990

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Search Results

Deafness, Autosomal Recessive 42 (DFNB42) via the ILDR1 Gene

Congenital Adrenal Hyperplasia (CAH) due to 11-β-Hydroxylase Deficiency (11-OHD) via the CYP11B1 Gene

Holoprosencephaly-11 via the CDON Gene

Cataract Type 11 via the PITX3 Gene

Spastic Paraplegia 11 via the SPG11 Gene

Lethal Congenital Contracture Arthrogryposis 11 via the GLDN Gene

Krabbe Disease via the GALC Exons 11-17 (502T/Del)

Primary Microcephaly, Autosomal Recessive, via the WDR62 Gene

Nephronophthisis / Senior-Loken Syndrome and Bardet-Biedl Syndrome via the SDCCAG8 Gene

Smith-Magenis and Potocki-Lupski syndromes via the RAI1 Gene

Autosomal Dominant Retinitis Pigmentosa 17 (RP17) via the CA4 Gene

Late-Onset Autosomal Dominant Retinitis Pigmentosa 42 (RP42) and Crisponi/Cold-Induced Sweating Syndrome Type 1(CISS1)-Like Phenotype Associated with Early-Onset Autosomal Recessive Retinitis Pigmentosa via the KLHL7 Gene

Retinitis Pigmentosa via the IMPDH1 Gene

RLBP1-Related Disorders via the RLBP1 Gene

X-Linked Spondyloepiphyseal Dysplasia Tarda (SEDT) via the TRAPPC2 Gene

Leber Congenital Amaurosis via the CRX Gene

Isolated Nonsyndromic Congenital Heart Defects via the NKX2-5 Gene

Myofibrillar Myopathy via the LDB3 (ZASP) Gene

Hereditary Spherocytosis via the EPB42 Gene

Medium Chain Acyl-CoA Dehydrogenase Deficiency via the ACADM Gene