Alzheimer's Disease, Familial, Plus APOE Panel PreventionGenetics, part of Exact Sciences
United States | 5 | 4 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
PSEN1 - NGS including CNV analysis Centogene AG - the Rare Disease Company
Germany | 5 | 1 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
CentoNeuro Panel Centogene AG - the Rare Disease Company
Germany | 1886 | 1858 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
Epilepsy Panel Centogene AG - the Rare Disease Company
Germany | 734 | 744 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
CentoIEM Panel Centogene AG - the Rare Disease Company
Germany | 669 | 688 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
Parkinson Disease Panel Centogene AG - the Rare Disease Company
Germany | 78 | 76 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
Amyotrophic Lateral Sclerosis (ALS) / Dementia Panel Centogene AG - the Rare Disease Company
Germany | 64 | 66 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
CentoCardio Panel Centogene AG - the Rare Disease Company
Germany | 289 | 275 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
Stroke, Cerebral Hemorrhage, Hemiplegia, and Migraine Panel PreventionGenetics, part of Exact Sciences
United States | 346 | 160 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Invitae Hereditary Amyotrophic Lateral Sclerosis, Frontotemporal Dementia and Alzheimer Disease Panel Labcorp Genetics (formerly Invitae) LabCorp
United States | 72 | 33 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
|
Dementia, Plus APOE Panel PreventionGenetics, part of Exact Sciences
United States | 27 | 19 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Amyotrophic Lateral Sclerosis (ALS) and Frontotemporal Dementia (FTD) Panel PreventionGenetics, part of Exact Sciences
United States | 45 | 38 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Alzheimer disease, type 3, with spastic paraparesis and apraxia, 607822, Autosomal dominant; AD (Early-onset autosomal dominant Alzheimer disease) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - D Deletion/duplication analysis
|
Alzheimer disease, type 3, with spastic paraparesis and apraxia, 607822, Autosomal dominant; AD (Early-onset autosomal dominant Alzheimer disease) (PSEN1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Alzheimer disease, type 3, with spastic paraparesis and unusual plaques, 607822, Autosomal dominant; AD (Early-onset autosomal dominant Alzheimer disease) (PSEN1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Alzheimer disease, type 3, with spastic paraparesis and unusual plaques, 607822, Autosomal dominant; AD (Early-onset autosomal dominant Alzheimer disease) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - D Deletion/duplication analysis
|
Alzheimer disease, type 3, 607822, Autosomal dominant; AD (Early-onset autosomal dominant Alzheimer disease) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - D Deletion/duplication analysis
|
Alzheimer disease, type 3, 607822, Autosomal dominant; AD (Early-onset autosomal dominant Alzheimer disease) (PSEN1 gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
|
Parkinson Disease and Parkinsonism Panel PreventionGenetics, part of Exact Sciences
United States | 70 | 71 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
|
Ataxia Exome Genetic Services Laboratory University of Chicago
United States | 294 | 481 | - C Sequence analysis of the entire coding region
|
