Search Tests - PreventionGenetics

Menu

Menu
  • Testing

      Test Menu

      • PGnome
      • PGxome
      • PGmax
      • Custom Panels
      • Tests by Category
      • How To Order
      • Targeted Variants
      • Prenatal
      • All Tests
      • Tests by Disease

      Test Information

      • Test Methods
      • Variant Interpretation
      • Family Testing
      • Re-analysis Policy
      • Extract and Hold
  • Sponsored Testing

      Partner Programs

      • Collaboration
      • Sponsored Testing
      • Clinical Trials and Research Studies
  • Billing

      Billing Information

      • Billing Policy
      • In-network Health Plans
      • Utilization Management
      • FAQs
      • Forms
  • How to Order

      Process

      • Log In / myPrevent
      • Ordering Instructions
      • Ordering Instructions
      • Report Retrieval
      • Turnaround Time
      • Forms
      • Order Kits

      Additional Info

      • Specimens & Shipping
      • Sample Reports
      • FAQs
      • Sending NY Specimens
      • Family Follow-up Testing
  • About Us

      PreventionGenetics

      • About PreventionGenetics
      • Genetics Experts
      • Quality & Value
      • Publications
      • Licenses and Certificates
      • Webinars
      • PGNewsroom
      • Join Our Team
  • Contact Us
  • Forms
    • 0

    • Log In / Sign Up

      myPrevent

  • Menu
HOME | CONTACT US | FORMS |

Log In / Sign Up

myPrevent

|

0

  • Testing

      Test Menu

      • PGnome
      • PGxome
      • PGmax
      • Custom Panels
      • Tests by Category
      • How To Order
      • Targeted Variants
      • Prenatal
      • All Tests
      • Tests by Disease

      Test Information

      • Test Methods
      • Variant Interpretation
      • Family Testing
      • Re-analysis Policy
      • Extract and Hold
  • |
  • Sponsored Testing

      Partner Programs

      • Collaboration
      • Sponsored Testing
      • Clinical Trials and Research Studies
  • |
  • Billing

      Billing Information

      • Billing Policy
      • In-network Health Plans
      • Utilization Management
      • FAQs
      • Forms
  • |
  • How to Order

      Process

      • Log In / myPrevent
      • Ordering Instructions
      • Ordering Instructions
      • Report Retrieval
      • Turnaround Time
      • Forms
      • Order Kits

      Additional Info

      • Specimens & Shipping
      • Sample Reports
      • FAQs
      • Sending NY Specimens
      • Family Follow-up Testing
  • |
  • About Us

      PreventionGenetics

      • About PreventionGenetics
      • Genetics Experts
      • Quality & Value
      • Publications
      • Licenses and Certificates
      • Webinars
      • PGNewsroom
      • Join Our Team

Browser Upgrade Recommended. More Info

We have detected that you are using Internet Explorer or Microsoft Edge Legacy. Please consider upgrading your browser to any of the following for the best experience.

  • Google Chrome
  • Firefox
  • Microsoft Edge
  • Safari

Login

Forgot username?

Forgot password?

Don't have an account?

×
  • Test By Category
  • View All Tests
  • View All Panels

FILTERS

ORDER
Test Kits

RESULTS KEY

  • Tests & Panels
  • Categories
  • Newsroom
  • Custom panels
  • Pages & Documents
  • Webinars

Searched: Rhizomelic Chondrodysplasia Punctata Type 2 via the GNPAT Gene

Search Results

  • DNA in a shopping cart Peroxisomal Disorders Panel
    Test Code
    Method
    Price
    10369
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Severe Skeletal Conditions Panel
    Test Code
    Method
    Price
    15771
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Comprehensive Cataracts Panel
    Test Code
    Method
    Price
    12001
    Sequencing with CNV PGxome
    $1290
  • DNA in a shopping cart Anterior Segment Dysgenesis Disorders Panel
    Test Code
    Method
    Price
    12003
    Sequencing with CNV PGxome
    $1290
  • DNA in a shopping cart Lysosomal Storage Disorders Panel
    Test Code
    Method
    Price
    13065
    Sequencing with CNV PGxome
    $1290
  • DNA in a shopping cart Conradi-Hunermann syndrome via the EBP Gene
    Test Code
    Method
    Price
    8935
    Sequencing with CNV PGxome
    $990
    781
    Sanger Sequencing
    $560
  • DNA in a shopping cart Chondrodysplasia Punctata 1, X-Linked Recessive (CDPX1) via the ARSL/ARSE Gene
    Test Code
    Method
    Price
    9935
    Sequencing with CNV PGxome
    $990
    813
    Sanger Sequencing
    $790
  • DNA in a shopping cart PGmaxTM - Skeletal Disorders and Joint Problems Panel
    Test Code
    Method
    Price
    10631
    Sequencing with CNV PGxome
    $1790
  • DNA in a shopping cart Non-Immune Hydrops Fetalis Panel
    Test Code
    Method
    Price
    12661
    Sequencing with CNV PGxome
    $1290
  • DNA in a shopping cart Metaphyseal Chondrodysplasia, Schmid Type (MCDS) via the COL10A1 Gene
    Test Code
    Method
    Price
    8771
    Sequencing with CNV PGxome
    $990
    802
    Sanger Sequencing
    $610
  • DNA in a shopping cart Cholestasis Panel
    Test Code
    Method
    Price
    10319
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart PGmaxTM - Comprehensive Ocular Disorders Panel
    Test Code
    Method
    Price
    12005
    Sequencing with CNV PGxome
    $1790
  • DNA in a shopping cart Inherited Ichthyoses and Related Disorders Panel
    Test Code
    Method
    Price
    4929
    Sequencing with CNV PGxome
    $990
  • News News

    …• Apert Syndrome • Chondrodysplasia Punctata • Cleidocranial Dysostosis • Cornelia de Lange syndrome and Cornelia de Lange –related conditions • Cranioectodermal Dysplasia Craniosynostosis • Ehlers-Danlos Syndrome • Ellis-van Creveld Syndrome…

  • DNA in a shopping cart Neurofibromatosis Type 2 via the NF2 Gene
    Test Code
    Method
    Price
    4041
    Sequencing with CNV PG-Select
    $990
  • DNA in a shopping cart Sterol Disorders Panel
    Test Code
    Method
    Price
    13319
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Renal Hypouricemia Type 2 via the SLC2A9 Gene
    Test Code
    Method
    Price
    2028
    Sanger Sequencing
    $940
    8181
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Wolfram Syndrome Type 2 via the CISD2 Gene
    Test Code
    Method
    Price
    1478
    Sanger Sequencing
    $440
    10045
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Cataract Type 2 (CTRCT2) via the CRYGC Gene
    Test Code
    Method
    Price
    2211
    Sanger Sequencing
    $490
    3891
    Sequencing with CNV PGxome
    $990
  • DNA in a shopping cart Bartter Syndrome Type 2 via the KCNJ1 Gene
    Test Code
    Method
    Price
    1266
    Sanger Sequencing
    $610
    8723
    Sequencing with CNV PGxome
    $990
1 2 3 4 5 6 7 8 9 10 Next
  • GO BACK
    Test By Category
  • View All Tests
  • View All Panels
ORDER
Test Kits
Custom Panel CogSTART
Custom Panel

RESULTS KEY

  • Tests & Panels
  • Categories
  • Newsroom
  • Custom panels
  • Pages & Documents
  • Webinars

PreventionGenetics,
A wholly owned subsidiary of Exact Sciences Corp.

3800 S. Business Park Ave.
Marshfield, WI 54449
Contact Us

© 2025 PreventionGenetics. All rights reserved.

Quick links

Privacy Practices & Policies
HIPAA Compliance
Do Not Sell
Contact Us
Careers
Get on Our Mailing List

Follow us on