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Results: 1 to 20 of 20
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
ASXL1 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 2 | 1 |
|
PreventionGenetics, part of Exact Sciences United States | 285 | 137 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
PreventionGenetics, part of Exact Sciences United States | 48 | 28 |
|
Bohring-Opitz Syndrome via the ASXL1 Gene PreventionGenetics, part of Exact Sciences United States | 1 | 1 |
|
Cornelia de Lange Syndrome and Cornelia de Lange Syndrome-Related Disorders Panel PreventionGenetics, part of Exact Sciences United States | 43 | 42 |
|
MNG Laboratories (Medical Neurogenetics, LLC.) United States | 414 | 800 |
|
Periventricular heterotopia panel Genologica Medica Spain | 52 | 20 |
|
Duzen Laboratories Duzen BBAGUAS Turkey | 2 | 1 |
|
Al Jalila Children's Genomics Center Al Jalila Childrens Speciality Hospital United Arab Emirates | 10 | 10 |
|
Bohring-Opitz Syndrome (ASXL1 Single Gene Test) Fulgent Genetics United States | 2 | 1 |
|
Bohring-Opitz Syndrome: gene sequencing CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 | 1 |
|
Bohring-Opitz Syndrome , Sequencing ASXL1 Gene Reference Laboratory Genetics Spain | 1 | 1 |
|
Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 26 | 22 |
|
Cornelia de Lange Syndrome Panel Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 10 | 10 |
|
CeGaT GmbH Germany | 2 | 1 |
|
Fulgent Genetics United States | 2 | 1 |
|
Fulgent Genetics United States | 5127 | 4672 |
|
Intellectual Disability NGS Panel Fulgent Genetics United States | 1057 | 554 |
|
Results: 1 to 20 of 20
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.