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Results: 1 to 15 of 15
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
CCDC8 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Invitae Skeletal Disorders Panel Invitae United States | 624 | 349 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Three M syndrome Comprehensive panel HNL Genomics Connective Tissue Gene Tests United States | 3 | 3 |
|
Three M syndrome Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests United States | 3 | 3 |
|
HNL Genomics Connective Tissue Gene Tests United States | 3 | 3 |
|
3-M Syndrome via the CCDC8 Gene PreventionGenetics United States | 1 | 1 |
|
3M syndrome / primordial dwarfism panel. NGS panel of 24 genes. Genologica Medica Spain | 33 | 24 |
|
Comprehensive Short Stature Genetic Panel MNG Laboratories (Medical Neurogenetics, LLC.) United States | 82 | 60 |
|
Fulgent Genetics United States | 21 | 16 |
|
3M Syndrome , Panel Massive Sequencing (NGS) CUL7, OBSL1, CCDC8 Genes Reference Laboratory Genetics Spain | 3 | 3 |
|
Selected Genetic Syndromes with skeletal involvement Panel CeGaT GmbH Germany | 36 | 42 |
|
Fulgent Genetics United States | 1 | 1 |
|
Fulgent Genetics United States | 5129 | 4672 |
|
Results: 1 to 15 of 15
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