Panels

Genetic testing for

Panels

RefLab Genetics
/
Panels

Genetic testing for

Panels

RefLab Genetics
/
Panels

Continually updated panels using HPO in order to include the most recent association published between phenotype and genotype.

Lower number of VOUS thanks to our database Reflab Database®, and main genetic variants and specific to illness databases.

The best turnaround times (< 30 days).

Pre and postanalysis support with our experts in clinical genetics.

Conclusive, transparent and customizable clinical reports.

Maximum diagnostic yield and clinical utility.

Download information

Request and consent form
Request and consent form
Report example

Ask us more

    Explore our Panels panels

    Search

    More results...

    Generic filters


    See all NGS panels

    ZINSSER-COLE-ENGMAN SYNDROME
    ZIMMERMANN-LABAND SYNDROME , NEXT-GENERATION SEQUENCING (NGS) ATP6V1B2 AND KCNH1 GENES
    ZELLWEGER SYNDROME TYPE 5A , SEQUENCING PEX2 GENE
    ZELLWEGER SYNDROME TYPE 8A , SEQUENCING PEX16 GENE
    ZELLWEGER SYNDROME TYPE 6A , SEQUENCING PEX10 GENE
    ZINC DEFICIENCY IN BREAST MILK , SEQUENCING SLC30A2 GENE

    Do you need more information?

    Are you a verified customer?

    Check our sample requirements

    Contact us at
    genetics@referencelaboratory.es

    Ordering a test or Service from
    us is simple and quick

    We have optimized all our processes to accept a wide range of samples, always adapting to each case.
    See sample requirements

    Do you need more information?

    Contact us at
    genetics@referencelaboratory.es

    Are you a verified customer?

    Ordering a test or Service from
    us is simple and quick

    Check our sample requirements

    We have optimized all our processes to accept a wide range of samples, always adapting to each case.
    See sample requirements

    Get our latest updates
    directly to your mailbox

      Continually updated panels using HPO in order to include the most recent association published between phenotype and genotype.

      Lower number of VOUS thanks to our database Reflab Database®, and main genetic variants and specific to illness databases.

      The best turnaround times (< 30 days).

      Pre and postanalysis support with our experts in clinical genetics.

      Conclusive, transparent and customizable clinical reports.

      Maximum diagnostic yield and clinical utility.

      Download information

      Request and consent form
      Request and consent form
      Report example

      Ask us more

        Explore our Panels panels

        Search

        More results...

        Generic filters


        See all NGS panels

        ZINSSER-COLE-ENGMAN SYNDROME
        ZIMMERMANN-LABAND SYNDROME , NEXT-GENERATION SEQUENCING (NGS) ATP6V1B2 AND KCNH1 GENES
        ZELLWEGER SYNDROME TYPE 5A , SEQUENCING PEX2 GENE
        ZELLWEGER SYNDROME TYPE 8A , SEQUENCING PEX16 GENE
        ZELLWEGER SYNDROME TYPE 6A , SEQUENCING PEX10 GENE
        ZINC DEFICIENCY IN BREAST MILK , SEQUENCING SLC30A2 GENE

        Do you need more information?

        Are you a verified customer?

        Check our sample requirements

        Contact us at
        genetics@referencelaboratory.es

        Ordering a test or Service from
        us is simple and quick

        We have optimized all our processes to accept a wide range of samples, always adapting to each case.
        See sample requirements

        Do you need more information?

        Contact us at
        genetics@referencelaboratory.es

        Are you a verified customer?

        Ordering a test or Service from
        us is simple and quick

        Check our sample requirements

        We have optimized all our processes to accept a wide range of samples, always adapting to each case.
        See sample requirements

        Get our latest updates
        directly to your mailbox

          error: Content is protected
          ×