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GTR Home > Tests > NeurodevelopmentNext-Expanded™

Overview

Test order codeHelp: 6860

Test name

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NeurodevelopmentNext-Expanded™

Purpose of the test

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This is a clinical test intended for Help: Diagnosis, Pre-symptomatic

Condition

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Click Indication tab for more information.

How to order

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Order URL Help: http://www.ambrygen.com/clinician/ordering-process

Specimen source

Amniocytes
Bone marrow
Buccal swab
Buffy coat
Cell culture
Chorionic villi
Cord blood
Dried blood spot (DBS) card
Fetal blood
Fibroblasts
Isolated DNA
Semen
Peripheral (whole) blood
Product of conception (POC)
Saliva

Methodology

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Molecular Genetics
DDeletion/duplication analysis
Next-Generation (NGS)/Massively parallel sequencing (MPS)
CSequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)

Summary of what is tested

Click Methodology tab for more information.

Clinical utility

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Not provided

Clinical validity

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Clinical validity depends on specific clinical and family history.

Citations

Not provided

Test services

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  • Clinical Testing/Confirmation of Mutations Identified Previously, Order code: 5640

Clinical resources

Practice guidelines

  • ACMG, 2016
    Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
  • ASHG/ACMG, 2015
    Points to Consider: Ethical, Legal, and Psychosocial Implications of Genetic Testing in Children and Adolescents
  • ACMG, 2015
    Clinical utility of genetic and genomic services: a position statement of the American College of Medical Genetics and Genomics.
  • ACMG, 2015
    Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology.
  • ACMG, 2013
    ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.

Consumer resources

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.