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Results: 41 to 60 of 69

Tests names and labsConditionsGenes, analytes, and microbesMethods

Apert Syndrome (FGFR2 Single Gene Test)

Fulgent Genetics
United States
111
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Facial Dysostosis and Related Disorders NGS Panel

Fulgent Genetics
United States
8529
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Craniosynostosis NGS Panel

Fulgent Genetics
United States
33961
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Kidney Dysplasia NGS Panel

Fulgent Genetics
United States
6841
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Beare-Stevenson Cutis Gyrata Syndrome (FGFR2 Single Gene Test)

Fulgent Genetics
United States
111
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hearing Loss Advanced Sequencing and CNV Evaluation

Athena Diagnostics Inc
United States
249184
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

APERT SYNDROME

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Apert Syndrome, Deletions-Duplications (MLPA) FGFR2 Gene

Reference Laboratory Genetics
Spain
11
  • D Deletion/duplication analysis

Apert Syndrome , Sequencing FGFR2 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

PreSeek Non-invasive Prenatal Gene Sequencing Screen

Baylor Genetics
United States
4930
  • C Sequence analysis of the entire coding region

FGFR2-Related disorders: FGFR2 Targeted Analysis

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
51
  • E Sequence analysis of select exons

Invitae Craniosynostosis Panel

Invitae
United States
149
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FGFR2 - Gene sequencing

Amsterdam UMC Genome Diagnostics Amsterdam University Medical Center
Netherlands
51
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Apert syndrome

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Single gene testing FGFR2

CeGaT GmbH
Germany
111
  • C Sequence analysis of the entire coding region

FGFR2

Institute of Human Genetics Medical University Innsbruck
Austria
21
  • S Mutation scanning of the entire coding region

FGFR2 Single Gene

Fulgent Genetics
United States
111
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasias NGS Panel

Fulgent Genetics
United States
543178
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FGFR-Related Craniosynostosis NGS Panel

Fulgent Genetics
United States
253
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasia

Asper Biogene Asper Biogene LLC
Estonia
16674
  • C Sequence analysis of the entire coding region

Results: 41 to 60 of 69

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.