Leigh syndrome due to mitochondrial complex I deficiency, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (FOXRED1 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Leigh syndrome due to mitochondrial complex 1 deficiency, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (NDUFA12 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Leigh syndrome, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (NDUFAF2 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
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Leigh syndrome, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (NDUFA10 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Leigh syndrome due to mitochondrial COX4 deficiency, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (COX10 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
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Leigh syndrome, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (NDUFS4 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
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Leigh syndrome, due to COX IV deficiency, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (SURF1 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
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Leigh syndrome due to mitochondrial complex I deficiency, 256000, Autosomal recessive, Mitochondrial (Isolated complex I deficiency) (NDUFS3 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
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Leigh syndrome due to mitochondrial complex I deficiency, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (NDUFAF6 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
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Leigh syndrome due to mitochondrial complex I deficiency, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (NDUFS8 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Leigh syndrome, due to COX IV deficiency, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (SURF1 gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Leigh syndrome, 256000, Autosomal recessive, Mitochondrial (Leigh syndrome) (SDHA gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey | 1 | 1 | - C Sequence analysis of the entire coding region
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Hereditary Cancer Screening - Colorectal & Gastric Cancer Panel (including Pancreatic Cancer) - (43 Genes) Genesys Diagnostics Genesys Diagnostics, Inc.
United States | 58 | 43 | - X Mutation scanning of select exons
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Hereditary Cancer Screening - Common Hereditary Cancer Panel (41 Genes) Genesys Diagnostics Genesys Diagnostics, Inc.
United States | 47 | 41 | - X Mutation scanning of select exons
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Hereditary Cancer Screening - Nervous System & Endocrine Cancer Panel (44 Genes) Genesys Diagnostics Genesys Diagnostics, Inc.
United States | 52 | 44 | - X Mutation scanning of select exons
|
Hereditary Cancer Screening - Renal/Urinary Tract Cancer Panel (Including prostate and kidney cancer) - (39 Genes) Genesys Diagnostics Genesys Diagnostics, Inc.
United States | 40 | 39 | - X Mutation scanning of select exons
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Hereditary Cancer Screening - Full Hereditary Cancer Panel (99 Genes) Genesys Diagnostics Genesys Diagnostics, Inc.
United States | 109 | 99 | - X Mutation scanning of select exons
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Cardiology Sequencing- Arrhythmia Comprehensive Panel (134 Genes) Genesys Diagnostics Genesys Diagnostics, Inc.
United States | 88 | 134 | - X Mutation scanning of select exons
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Cardiology Sequencing- Full Panel (174 Genes) Genesys Diagnostics Genesys Diagnostics, Inc.
United States | 122 | 174 | - X Mutation scanning of select exons
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Carrier Screening - Comprehensive Panel (145 Genes) Genesys Diagnostics Genesys Diagnostics, Inc.
United States | 185 | 145 | - D Deletion/duplication analysis
- I Microsatellite instability testing (MSI)
- X Mutation scanning of select exons
- T Targeted variant analysis
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