U.S. flag

An official website of the United States government

GTR Home > Tests > Pfeiffer syndrome, 101600, Autosomal dominant (Pfeiffer syndrome) (FGFR1 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Overview

Test order codeHelp: 12474

Test name

Help

Pfeiffer syndrome, 101600, Autosomal dominant (Pfeiffer syndrome) (FGFR1 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Purpose of the test

Help

This is a clinical test intended for Help: Diagnosis

Condition

Help

Loading data ......

Click Indication tab for more information.

How to order

Help

Not provided

Methodology

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

Summary of what is tested

Loading data ......

Click Methodology tab for more information.

Clinical utility

Help

Not provided

Clinical validity

Help

Not provided

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.