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Searched: Galloway Mowat Syndrome (GAMOS) via the GON7��Gene

Search Results

Sick Sinus Syndrome and Brugada Syndrome via the HCN4 Gene

Test Code

Method

Price

11369

Sequencing with CNV PGxome

$890

947

Sanger Sequencing

$960
Oculofaciocardiodental Syndrome and Lenz Microphthalmia Syndrome via the BCOR Gene

Test Code

Method

Price

11105

Sequencing with CNV PGxome

$890

949

Sanger Sequencing

$1250
Pierson Syndrome and Congenital Nephrotic Syndrome via the LAMB2 Gene

Test Code

Method

Price

11443

Sequencing with CNV PGxome

$890

556

Sanger Sequencing

$1620
Crigler-Najjar Syndrome and Gilbert Syndrome via the UGT1A1 Gene

Test Code

Method

Price

7851

Sequencing with CNV PG-Select

$640
Meckel-Gruber Syndrome / Joubert Syndrome via the TCTN2 Gene

Test Code

Method

Price

576

Sanger Sequencing

$1010

11041

Sequencing with CNV PGxome

$890
Top 99 Genetic Causes of Developmental Delay Panel

Test Code

Method

Price

12675

Sequencing with CNV PGxome

$990
Joubert Syndrome, Meckel-Gruber Syndrome, and Nephronophthisis via the TMEM67 Gene

Test Code

Method

Price

15205

Sequencing with CNV PG-Select

$640
Temple-Baraitser Syndrome and Zimmermann-Laband Syndrome via the KCNH1 Gene

Test Code

Method

Price

8081

Sequencing with CNV PG-Select

$640
Congenital Variant Rett syndrome or FOXG1 syndrome via the FOXG1 Gene

Test Code

Method

Price

8637

Sequencing with CNV PG-Select

$640
Andersen-Tawil Syndrome/Long QT Syndrome via the KCNJ2 Gene

Test Code

Method

Price

1042

Sanger Sequencing

$440

9163

Sequencing with CNV PGxome

$890
Atypical Hemolytic-Uremic Syndrome and Nephrotic Syndrome via the DGKE Gene

Test Code

Method

Price

11227

Sequencing with CNV PGxome

$890

1507

Sanger Sequencing

$910
Differences of Sex Development (DSD) Panel

Test Code

Method

Price

4509

Sequencing with CNV PGxome

$1240
Van Maldergem Syndrome (Cerebro-Facio-Articular Syndrome) via the DCHS1 Gene

Test Code

Method

Price

2530

Sanger Sequencing

$1900

7987

Sequencing with CNV PGxome

$890
Nephronophthisis / Senior-Loken Syndrome and Bardet-Biedl Syndrome via the SDCCAG8 Gene

Test Code

Method

Price

15197

Sequencing with CNV PG-Select

$640
Cornelia de Lange Syndrome and Wiedemann-Steiner Syndrome via the KMT2A Gene

Test Code

Method

Price

11437

Sequencing with CNV PGxome

$890

2591

Sanger Sequencing

$2670
Long QT Syndrome and Jervell and Lange-Nielsen Syndrome via the KCNE1 Gene

Test Code

Method

Price

1043

Sanger Sequencing

$440

9193

Sequencing with CNV PGxome

$890
Long QT Syndrome and Jervell and Lange-Nielsen syndrome via the KCNQ1 Gene

Test Code

Method

Price

11421

Sequencing with CNV PGxome

$890

1040

Sanger Sequencing

$1020
Stickler Syndrome Type II, Marshall Syndrome, and Fibrochondrogenesis via the COL11A1 Gene

Test Code

Method

Price

11187

Sequencing with CNV PGxome

$890

831

Sanger Sequencing

$2490
Nevoid Basal Cell Carcinoma Syndrome/Gorlin Syndrome via the PTCH1 Gene

Test Code

Method

Price

10673

Sequencing with CNV PG-Select

$540
Noonan Syndrome via the SOS2 Gene

Test Code

Method

Price

4365

Sequencing with CNV PG-Select

$640

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Search Results

Sick Sinus Syndrome and Brugada Syndrome via the HCN4 Gene

Oculofaciocardiodental Syndrome and Lenz Microphthalmia Syndrome via the BCOR Gene

Pierson Syndrome and Congenital Nephrotic Syndrome via the LAMB2 Gene

Crigler-Najjar Syndrome and Gilbert Syndrome via the UGT1A1 Gene

Meckel-Gruber Syndrome / Joubert Syndrome via the TCTN2 Gene

Top 99 Genetic Causes of Developmental Delay Panel

Joubert Syndrome, Meckel-Gruber Syndrome, and Nephronophthisis via the TMEM67 Gene

Temple-Baraitser Syndrome and Zimmermann-Laband Syndrome via the KCNH1 Gene

Congenital Variant Rett syndrome or FOXG1 syndrome via the FOXG1 Gene

Andersen-Tawil Syndrome/Long QT Syndrome via the KCNJ2 Gene

Atypical Hemolytic-Uremic Syndrome and Nephrotic Syndrome via the DGKE Gene

Differences of Sex Development (DSD) Panel

Van Maldergem Syndrome (Cerebro-Facio-Articular Syndrome) via the DCHS1 Gene

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

Cornelia de Lange Syndrome and Wiedemann-Steiner Syndrome via the KMT2A Gene

Long QT Syndrome and Jervell and Lange-Nielsen Syndrome via the KCNE1 Gene

Long QT Syndrome and Jervell and Lange-Nielsen syndrome via the KCNQ1 Gene

Stickler Syndrome Type II, Marshall Syndrome, and Fibrochondrogenesis via the COL11A1 Gene

Nevoid Basal Cell Carcinoma Syndrome/Gorlin Syndrome via the PTCH1 Gene

Noonan Syndrome via the SOS2 Gene