Filters
Other countries
Results: 1 to 16 of 16
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Invitae Skeletal Disorders Panel Invitae United States | 624 | 349 |
|
Parietal foramina 1, 168500, Autosomal dominant; PFM1 (Enlarged parietal foramina) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins Hospital United States | 110 | 45 |
|
PreventionGenetics, part of Exact Sciences United States | 177 | 163 |
|
Craniosynostosis via the MSX2 Gene PreventionGenetics, part of Exact Sciences United States | 3 | 1 |
|
MNG Laboratories (Medical Neurogenetics, LLC.) United States | 414 | 800 |
|
Institute for Human Genetics University Medical Center Freiburg Germany | 3 | 1 |
|
Parietal foramina 1, Craniosynostosis type 2 (sequence analysis of MSX2 gene) CGC Genetics Unilabs Portugal | 2 | 1 |
|
Craniosynostosis panel. NGS panel of 37 genes. Genologica Medica Spain | 113 | 37 |
|
Skeletal diseases. NGS panel of 169 genes. Genologica Medica Spain | 373 | 169 |
|
Parietal foramina: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 2 | 2 |
|
Fulgent Genetics United States | 339 | 61 |
|
Laboratorio de Genetica Clinica SL Spain | 1 | 1 |
|
Fulgent Genetics United States | 3 | 1 |
|
Fulgent Genetics United States | 5128 | 4672 |
|
Results: 1 to 16 of 16
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.