U.S. flag

An official website of the United States government

Filters

Test type

Test purpose

Test method

Test service

Laboratory certification

Specimen type

See more specimen types...

Laboratory location

Other countries

Results: 41 to 59 of 59

Tests names and labsConditionsGenes, analytes, and microbesMethods

Micromelic Dysplasia NGS Panel

Fulgent Genetics
United States
14024
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Thanatophoric Dysplasia (FGFR3 Single Gene Test)

Fulgent Genetics
United States
121
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SADDAN (FGFR3 Single Gene Test)

Fulgent Genetics
United States
121
  • 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

Hypochondroplasia (FGFR3 Single Gene Test)

Fulgent Genetics
United States
121
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neuronal Migration Disorders NGS Panel

Fulgent Genetics
United States
39283
  • 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

Metaphyseal Dysplasia NGS Panel

Fulgent Genetics
United States
3710
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Osteogenesis Imperfecta

Asper Biogene Asper Biogene LLC
Estonia
8041
  • C Sequence analysis of the entire coding region

Hearing Loss Advanced Sequencing and CNV Evaluation

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

Syndromic Craniosynostosis , Panel Massive Sequencing (NGS) 9 Genes

Reference Laboratory Genetics
Spain
139
  • C Sequence analysis of the entire coding region

Epilepsy Comprehensive NGS Panel

Fulgent Genetics
United States
729398
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Single gene testing FGFR3

CeGaT GmbH
Germany
141
  • C Sequence analysis of the entire coding region

FGFR3 Single Gene

Fulgent Genetics
United States
121
  • 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

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Camptodactyly, tall stature, and hearing loss syndrome

Institute of Human Genetics Cologne University
Germany
11
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Results: 41 to 59 of 59

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.