PlateletGenex Functional Defect Panel (31 genes) (2 Day STAT TAT) Machaon Diagnostics
United States | 26 | 31 | - C Sequence analysis of the entire coding region
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FGA - NGS including CNV analysis Centogene AG - the Rare Disease Company
Germany | 3 | 1 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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FGB - NGS including CNV analysis Centogene AG - the Rare Disease Company
Germany | 2 | 1 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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FGG - NGS including CNV analysis Centogene AG - the Rare Disease Company
Germany | 2 | 1 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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CentoImmuno Panel Centogene AG - the Rare Disease Company
Germany | 323 | 329 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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Blood Coagulation Panel Centogene AG - the Rare Disease Company
Germany | 110 | 112 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
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CentoICU Panel Centogene AG - the Rare Disease Company
Germany | 829 | 848 | - C Sequence analysis of the entire coding region
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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
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Dysfibrinogenemia Genetic Panel (2 Day STAT TAT) Machaon Diagnostics
United States | 2 | 3 | - C Sequence analysis of the entire coding region
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Hypofibrinogenemia, congenital, 202400, Autosomal recessive (Congenital fibrinogen deficiency) (FGG 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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Hypofibrinogenemia, congenital, 202400, Autosomal recessive (Congenital fibrinogen deficiency) (FGG 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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Hypofibrinogenemia, congenital, 202400, Autosomal recessive (Familial hypodysfibrinogenemia) (FGB 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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Hypofibrinogenemia, congenital, 202400, Autosomal recessive (Familial hypodysfibrinogenemia) (FGB 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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Afibrinogenemia, congenital, 202400, Autosomal recessive (Congenital fibrinogen deficiency) (FGG 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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Afibrinogenemia, congenital, 202400, Autosomal recessive (Familial afibrinogenemia) (FGB 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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Afibrinogenemia, congenital, 202400, Autosomal recessive (Congenital fibrinogen deficiency) (FGG 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
|
Afibrinogenemia, congenital, 202400, Autosomal recessive (Congenital fibrinogen deficiency) (FGA 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
|
Afibrinogenemia, congenital, 202400, Autosomal recessive (Congenital fibrinogen deficiency) (FGA 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
|
Afibrinogenemia, congenital, 202400, Autosomal recessive (Familial afibrinogenemia) (FGB 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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RenalZoom Johns Hopkins Genomics DNA Diagnostic Laboratory Johns Hopkins University, School of Medicine
United States | 525 | 338 | - C Sequence analysis of the entire coding region
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