Dihydropyrimidine Dehydrogenase Genotype Mayo Clinic Laboratories Mayo Clinic United States | 4 | 1 | - T Targeted variant analysis
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DPYD Full Gene Sequencing Mayo Clinic Laboratories Mayo Clinic United States | 4 | 1 | - C Sequence analysis of the entire coding region
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CentoMetabolic MOx Centogene AG - the Rare Disease Company Germany | 195 | 221 | - A Analyte
- D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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CentoScreen Centogene AG - the Rare Disease Company Germany | 316 | 314 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
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DPYD - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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Carrier Screening Guidelines-Based Panel Ambry Genetics United States | 199 | 165 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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CentoNeuro Panel Centogene AG - the Rare Disease Company Germany | 1886 | 1858 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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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
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Intellectual Disability Panel Centogene AG - the Rare Disease Company Germany | 777 | 770 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
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CentoIEM Panel Centogene AG - the Rare Disease Company Germany | 669 | 688 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
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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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Lysosomal Storage Disorders Panel PreventionGenetics United States | 242 | 146 | - D Deletion/duplication analysis
- C Sequence analysis of the entire coding region
- T Targeted variant analysis
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Dihydropyrimidine dehydrogenase deficiency, 274270, Autosomal recessive (Dihydropyrimidine dehydrogenase deficiency) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 | - D Deletion/duplication analysis
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Dihydropyrimidine dehydrogenase deficiency, 274270, Autosomal recessive (Dihydropyrimidine dehydrogenase deficiency) (DPYD 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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Dihydropyrimidine dehydrogenase deficiency, 274270, Autosomal recessive (Dihydropyrimidine dehydrogenase deficiency) (DPYD 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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Dihydropyrimidine dehydrogenase deficiency, 274270, Autosomal recessive (Dihydropyrimidine dehydrogenase deficiency) (Prenatal) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 | - D Deletion/duplication analysis
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5-fluorouracil toxicity, 274270, Autosomal recessive (Dihydropyrimidine dehydrogenase deficiency) (MLPA) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 | - D Deletion/duplication analysis
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5 fluorouracil toxicity (DPD gene - Allel 2A-IVS14+1G-A and *3,*4,*5A,*7,*8,*9,*10,*12,*13, M166V, R886H, D949V allels) (SnapShot analysis) (DPYD 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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5-fluorouracil toxicity, 274270, Autosomal recessive (Dihydropyrimidine dehydrogenase deficiency) (DPYD 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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Pharmacogenomics Test Panel IU Genetic Testing Laboratories Indiana University School of Medicine United States | 8 | 13 | - T Targeted variant analysis
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