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Searched: Hermansky-Pudlak Syndrome Type 3 (HPS3) via the HPS3 Gene

Search Results

Hermansky-Pudlak Syndrome via the HPS3 Gene, Exon 1 Deletion

Test Code

Method

Price

759

Targeted Deletion

$350
Hermansky-Pudlak Syndrome (HPS) Panel

Test Code

Method

Price

10269

Sequencing with CNV PGxome

$990
Hermansky-Pudlak Syndrome Type 8 (HPS8) via the BLOC1S3 Gene

Test Code

Method

Price

9181

Sequencing with CNV PGxome

$990

768

Sanger Sequencing

$440
Hermansky-Pudlak Syndrome Type 7 (HPS7) via the DTNBP1 Gene

Test Code

Method

Price

11269

Sequencing with CNV PGxome

$990

767

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

$990
Inherited Platelet Function Disorder Panel

Test Code

Method

Price

10371

Sequencing with CNV PGxome

$990
Bleeding Disorders Panel

Test Code

Method

Price

10425

Sequencing with CNV PGxome

$990
Oculocutaneous Albinism and Hypopigmentation Panel

Test Code

Method

Price

10313

Sequencing with CNV PGxome

$990
Congenital Diarrhea and Enteropathies Panel

Test Code

Method

Price

12647

Sequencing with CNV PGxome

$1290
Lysosomal Storage Disorders Panel

Test Code

Method

Price

13065

Sequencing with CNV PGxome

$1290
Inherited Bone Marrow Failure Panel

Test Code

Method

Price

7359

Sequencing with CNV PGxome

$1490
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PGmax^TM - Inborn Errors of Immunity/Primary Immunodeficiency (PID) Panel

Test Code

Method

Price

13999

Sequencing with CNV PGxome

$1790
PGmax^TM - Primary Immunodeficiency and Malignancy Predisposition Panel

Test Code

Method

Price

19998

Sequencing with CNV PGxome

$1790
PGmax^TM - Comprehensive Ocular Disorders Panel

Test Code

Method

Price

12005

Sequencing with CNV PGxome

$1790
Familial Hemophagocytic Lymphohistiocytosis, X-linked Lymphoproliferative Disease via the SH2D1A Gene

Test Code

Method

Price

138

Sanger Sequencing

$490

10039

Sequencing with CNV PGxome

$990
Familial Hemophagocytic Lymphohistiocytosis, X-linked Lymphoproliferative Disease via the XIAP/BIRC4 Gene

Test Code

Method

Price

139

Sanger Sequencing

$650

9989

Sequencing with CNV PGxome

$990
PGmax^TM - Comprehensive Inherited Metabolic Disorders and Mitochondrial Disorders (Nuclear Genes only) Panel

Test Code

Method

Price

16006

Sequencing with CNV PGxome

$1790
Interstitial Lung Disease Panel

Test Code

Method

Price

5211

Sequencing with CNV PGxome

$1290

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Search Results

Hermansky-Pudlak Syndrome via the HPS3 Gene, Exon 1 Deletion

Hermansky-Pudlak Syndrome (HPS) Panel

Hermansky-Pudlak Syndrome Type 8 (HPS8) via the BLOC1S3 Gene

Hermansky-Pudlak Syndrome Type 7 (HPS7) via the DTNBP1 Gene

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

Inherited Platelet Function Disorder Panel

Bleeding Disorders Panel

Oculocutaneous Albinism and Hypopigmentation Panel

Congenital Diarrhea and Enteropathies Panel

Lysosomal Storage Disorders Panel

Inherited Bone Marrow Failure Panel

All

All

PGmax^TM - Inborn Errors of Immunity/Primary Immunodeficiency (PID) Panel

PGmax^TM - Primary Immunodeficiency and Malignancy Predisposition Panel

PGmax^TM - Comprehensive Ocular Disorders Panel

Familial Hemophagocytic Lymphohistiocytosis, X-linked Lymphoproliferative Disease via the SH2D1A Gene

Familial Hemophagocytic Lymphohistiocytosis, X-linked Lymphoproliferative Disease via the XIAP/BIRC4 Gene

PGmax^TM - Comprehensive Inherited Metabolic Disorders and Mitochondrial Disorders (Nuclear Genes only) Panel

Interstitial Lung Disease Panel