MVL Vision Panel Molecular Vision Laboratory
United States | 1358 | 1028 | - C Sequence analysis of the entire coding region
|
Invitae Corneal Dystrophies Panel Invitae
United States | 65 | 33 | - D Deletion/duplication analysis
|
Marfan Syndrome and Related Aortopathies Panel PreventionGenetics
United States | 40 | 38 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Invitae Glaucoma Panel Invitae
United States | 57 | 27 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
Marfan syndrome, Loeys-Dietz syndrome, Familial thoracic aortic aneurysms & dissections, and Related disorders Comprehensive panel HNL Genomics Connective Tissue Gene Tests
United States | 18 | 27 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Marfan syndrome, Loeys-Dietz syndrome, Familial thoracic aortic aneurysms & dissections, and Related disorders NGS panel HNL Genomics Connective Tissue Gene Tests
United States | 18 | 27 | - C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Marfan syndrome, Loeys-Dietz syndrome, Familial thoracic aortic aneurysms & dissections, and Related disorders Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests
United States | 18 | 27 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
Aortic aneurysm, familial thoracic 11, susceptibility to, 617349, Autosomal dominant (Congenital primary aphakia) (FOXE3 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Genetic Diagnosis and Research Centre
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Connective Tissue Disorders Panel PreventionGenetics
United States | 164 | 99 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Connective tissue disorder NGS panel HNL Genomics Connective Tissue Gene Tests
United States | 37 | 47 | - C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Connective tissue disorder Comprehensive panel HNL Genomics Connective Tissue Gene Tests
United States | 37 | 47 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Connective tissue disorder Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests
United States | 37 | 47 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
Marfan syndrome, Loeys-Dietz syndrome, Familial thoracic aortic aneurysms & dissections, and Related disorders NGS panel HNL Genomics Connective Tissue Gene Tests
United States | 18 | 27 | - C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Marfan syndrome, Loeys-Dietz syndrome, Familial thoracic aortic aneurysms & dissections, and Related disorders Deletion / Duplication panel HNL Genomics Connective Tissue Gene Tests
United States | 18 | 27 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
Marfan syndrome, Loeys-Dietz syndrome, Familial thoracic aortic aneurysms & dissections, and Related disorders Comprehensive panel HNL Genomics Connective Tissue Gene Tests
United States | 18 | 27 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Familial Thoracic Aortic Aneurysm and Dissection (TAAD) Panel PreventionGenetics
United States | 16 | 17 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Corneal Dystrophies Panel PreventionGenetics
United States | 40 | 27 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Invitae Aortopathy Comprehensive Panel Invitae
United States | 60 | 29 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
Glaucoma Panel PreventionGenetics
United States | 38 | 24 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Cataract panel. NGS panel of 69 genes. Genologica Medica
Spain | 146 | 69 | - C Sequence analysis of the entire coding region
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