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Results: 41 to 49 of 49

Tests names and labsConditionsGenes, analytes, and microbesMethods

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

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

Beare-Stevenson syndrome

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

Beare-Stevenson syndrome

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

Craniosynostosis: FGFR2 gene sequence analysis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
61
  • C Sequence analysis of the entire coding region

Craniosynostosis: FGFR1 gene (exon 7), FGFR2 gene (exon 7) and FGFR3 gene (exons 6, 8) sequence analysis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
53
  • 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

Results: 41 to 49 of 49

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.