Filters
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
TGFB1 Sequence Analysis (Familial Mutation/Variant Analysis) Baylor Genetics United States | 1 | 1 |
|
High Bone Mass Panel by Massively Parallel Sequencing (BCM-MitomeNGS) Baylor Genetics United States | 1 | 14 |
|
NewbornDx Advanced Sequencing Evaluation Athena Diagnostics United States | 1 | 1722 |
|
Camurati-Engelmann Disease (TGFB1 Single Gene Test) Fulgent Genetics United States | 2 | 1 |
|
Comprehensive Growth Disorders / Skeletal Dysplasias and Disorders Panel Blueprint Genetics Finland | 2 | 308 |
|
Comprehensive Skeletal Dysplasias and Disorders Panel Blueprint Genetics Finland | 1 | 246 |
|
Skeletal Dysplasias Core Panel Blueprint Genetics Finland | 1 | 111 |
|
Laboratorio de Genetica Clinica SL Spain | 1 | 1 |
|
Osteopetrosis and Dense Bone Dysplasia Panel Blueprint Genetics Finland | 1 | 25 |
|
Skeletal dysplasia with increased bone density Panel CeGaT GmbH Germany | 26 | 28 |
|
Fulgent Genetics United States | 2 | 1 |
|
Fulgent Genetics United States | 557 | 182 |
|
Fulgent Genetics United States | 5130 | 4674 |
|
Baylor Genetics United States | 842 | 637 |
|
Camurati-Engelmann Disease, TGFB1 GGA - Galil Genetic Analysis Israel | 1 | 1 |
|
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.