DVL1
Locus: 1p36.33
Protein: Dishevelled, dsh homolog 1
Disorders
Tests
TAT: 2-4 weeks Robinow syndrome NGS panelprice: $1,940.00 method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Connective Tissue Gene Tests - Allentown, PA, USA |
TAT: 2-3 weeks Robinow syndrome NGS panelprice: $850.00 method(s): ◦ Del/Dup (CNV) Connective Tissue Gene Tests - Allentown, PA, USA |
TAT: 2-3 weeks Robinow syndrome NGS panelprice: $1,190.00 method(s): ◦ Sequencing, Next Gen Connective Tissue Gene Tests - Allentown, PA, USA |
TAT: 1-2 weeks Robinow syndrome, autosomal dominant 2 (DRS2)price: $890.00 method(s): ◦ Sequencing, Capillary (Sanger) Connective Tissue Gene Tests - Allentown, PA, USA |
TAT: 2-3 weeks Robinow syndrome, autosomal dominant 2 (DRS2)price: $680.00 method(s): ◦ Del/Dup (CNV) Connective Tissue Gene Tests - Allentown, PA, USA |
TAT: 2-3 weeks Robinow syndrome, autosomal dominant 2 (DRS2)price: $1,470.00 method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Capillary (Sanger) Connective Tissue Gene Tests - Allentown, PA, USA |
| DVL1 method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) Fulgent Diagnostics - Temple City, CA, USA |
TAT: 1-2 weeks Robinow syndrome, autosomal dominant 2 (DRS2)price: $350.00 method(s): ◦ Sequencing, Capillary (Sanger) Connective Tissue Gene Tests - Allentown, PA, USA |
TAT: 1-2 weeks Robinow syndrome, autosomal dominant 2 (DRS2)price: $750.00 method(s): ◦ Sequencing, Capillary (Sanger) Connective Tissue Gene Tests - Allentown, PA, USA |
| Robinow syndrome, autosomal dominant type 2 method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) Centogene AG, Rare Disease Company - Rostock, Germany |
| Comprehensive Skeletal / Malformation Syndrome Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, Helsinki - Helsinki, Finland |
| Micromelic Dysplasia Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, Helsinki - Helsinki, Finland |
| Comprehensive Skeletal Dysplasias and Disorders Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, Helsinki - Helsinki, Finland |
| Skeletal Dysplasias Core Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, Helsinki - Helsinki, Finland |
| Comprehensive Skeletal / Malformation Syndrome Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, San Francisco - San Francisco, CA, USA |
| Micromelic Dysplasia Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, San Francisco - San Francisco, CA, USA |
| Comprehensive Skeletal Dysplasias and Disorders Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, San Francisco - San Francisco, CA, USA |
| Skeletal Dysplasias Core Panel method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen Blueprint Genetics, San Francisco - San Francisco, CA, USA |
