Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Craniosynostosis and Related Disorders Panel PreventionGenetics, part of Exact Sciences United States | 19 | 5 |
|
FGFR2-Related Disorders via the FGFR2 Gene PreventionGenetics, part of Exact Sciences United States | 8 | 1 |
|
Craniodysmorphology Screen (Targeted FGFR1,2, and 3) Center for Genetics at Saint Francis Saint Francis Hospital United States | 7 | 3 |
|
Craniosynostosis panel. NGS panel of 37 genes. Genologica Medica Spain | 113 | 37 |
|
Central skeletal dysplasias panel. NGS panel of 111 genes. Genologica Medica Spain | 258 | 111 |
|
Skeletal diseases. NGS panel of 169 genes. Genologica Medica Spain | 373 | 169 |
|
Crouzon syndrome: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 2 | 2 |
|
Duzen Laboratories Duzen BBAGUAS Turkey | 5 | 1 |
|
FGFR2 Deletion/duplication analysis Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center United States | 9 | 1 |
|
Custom XomeDx Slice – Differences of Sex Development (Proband Only) GeneDx United States | 21 | 112 |
|
Institute for Human Genetics University Medical Center Freiburg Germany | 11 | 1 |
|
Apert Syndrome (FGFR2 Single Gene Test) Fulgent Genetics United States | 11 | 1 |
|
Facial Dysostosis and Related Disorders NGS Panel Fulgent Genetics United States | 85 | 29 |
|
Fulgent Genetics United States | 339 | 61 |
|
Fulgent Genetics United States | 68 | 41 |
|
Beare-Stevenson Cutis Gyrata Syndrome (FGFR2 Single Gene Test) Fulgent Genetics United States | 11 | 1 |
|
FGFR2-related craniosynostosis: gene sequencing CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 7 | 1 |
|
Hearing Loss Advanced Sequencing and CNV Evaluation Athena Diagnostics United States | 249 | 184 |
|
Laboratorio de Genetica Clinica SL Spain | 1 | 1 |
|
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 47 | 44 |
|
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.