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Results: 81 to 95 of 95

Tests names and labsConditionsGenes, analytes, and microbesMethods

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

Hypogonadotropic Hypogonadism (HH) and Related Disorders NGS Panel

Fulgent Genetics
United States
2213
  • 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

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

Kallmann Syndrome NGS Panel

Fulgent Genetics
United States
2819
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pfeiffer syndrome

MedGene
Slovakia
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pfeiffer syndrome

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Pfeiffer syndrome

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Pfeiffer syndrome

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

FGFR1-related craniosynostosis

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

FGFR2-related craniosynostosis

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

FGFR2-Related Disorders: FGFR2 Sequencing

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
51
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons

Test for Pfeiffer syndrome

Genome Diagnostics Laboratory Hospital For Sick Children
Canada
12
  • E Sequence analysis of select exons

Results: 81 to 95 of 95

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.