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Searched: 426

Search Results

Distal Arthrogryposis 2B (Sheldon-Hall Syndrome) via the TNNT3 Gene

Test Code

Method

Price

11757

Sequencing with CNV PGxome

$990

334

Sanger Sequencing

$860
Distal Arthrogryposis 2B (Sheldon-Hall Syndrome) via the TNNI2 Gene

Test Code

Method

Price

333

Sanger Sequencing

$610

8741

Sequencing with CNV PGxome

$990
Giant Axonal Neuropathy via the GAN Gene

Test Code

Method

Price

11345

Sequencing with CNV PGxome

$990

918

Sanger Sequencing

$840
Restrictive Dermopathy and Mandibuloacral Dysplasia with Type B Lipodystrophy via the ZMPSTE24 Gene

Test Code

Method

Price

400

Sanger Sequencing

$710

8495

Sequencing with CNV PGxome

$990
Alzheimer's Disease, Familial or Cerebral Amyloid Angiopathy via the APP Gene

Test Code

Method

Price

4557

Sequencing with CNV PG-Select

$990
Peroxisome Biogenesis Disorders, Zellweger Syndrome Spectrum via the PEX1 Gene

Test Code

Method

Price

3087

Sequencing with CNV PG-Select

$990
Robinow Syndrome and Autosomal Recessive Brachydactyly, Type B1 via the ROR2 Gene

Test Code

Method

Price

8359

Sequencing with CNV PGxome

$990

136

Sanger Sequencing

$810
Colorectal Cancer Predisposition via the POLD1 Gene

Test Code

Method

Price

7509

Sequencing with CNV PG-Select

$990
Colorectal Cancer Predisposition via the POLE Gene

Test Code

Method

Price

7511

Sequencing with CNV PG-Select

$990
Nephronophthisis and Senior-Loken Syndrome via the IQCB1/NPHP5 Gene

Test Code

Method

Price

655

Sanger Sequencing

$790

9937

Sequencing with CNV PGxome

$990
Congenital Factor XIII deficiency via the F13A1 Gene

Test Code

Method

Price

11315

Sequencing with CNV PGxome

$990

2911

Sanger Sequencing

$970
Primary Microcephaly, Autosomal Recessive, via the CEP152 Gene

Test Code

Method

Price

921

Sanger Sequencing

$1490

8009

Sequencing with CNV PGxome

$990
Congenital Factor XIII Deficiency via the F13B Gene

Test Code

Method

Price

2912

Sanger Sequencing

$970

4147

Sequencing with CNV PGxome

$990
Ovarian Cancer and Rhabdoid Tumor Predisposition Syndrome via the SMARCA4 Gene

Test Code

Method

Price

3173

Sequencing with CNV PG-Select

$990
DOORS Syndrome and TBC1D24-related Epilepsy via the TBC1D24 Gene

Test Code

Method

Price

4261

Sequencing with CNV PG-Select

$990

Search Results

Distal Arthrogryposis 2B (Sheldon-Hall Syndrome) via the TNNT3 Gene

Distal Arthrogryposis 2B (Sheldon-Hall Syndrome) via the TNNI2 Gene

Giant Axonal Neuropathy via the GAN Gene

Restrictive Dermopathy and Mandibuloacral Dysplasia with Type B Lipodystrophy via the ZMPSTE24 Gene

Alzheimer's Disease, Familial or Cerebral Amyloid Angiopathy via the APP Gene

Peroxisome Biogenesis Disorders, Zellweger Syndrome Spectrum via the PEX1 Gene

Robinow Syndrome and Autosomal Recessive Brachydactyly, Type B1 via the ROR2 Gene

Colorectal Cancer Predisposition via the POLD1 Gene

Colorectal Cancer Predisposition via the POLE Gene

Nephronophthisis and Senior-Loken Syndrome via the IQCB1/NPHP5 Gene

Congenital Factor XIII deficiency via the F13A1 Gene

Primary Microcephaly, Autosomal Recessive, via the CEP152 Gene

Congenital Factor XIII Deficiency via the F13B Gene

Ovarian Cancer and Rhabdoid Tumor Predisposition Syndrome via the SMARCA4 Gene

DOORS Syndrome and TBC1D24-related Epilepsy via the TBC1D24 Gene