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Results: 1 to 15 of 15
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
KIF21A - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Centogene AG - the Rare Disease Company Germany | 1886 | 1858 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Strabismus Syndrome or Congenital Fibrosis of Extraocular Muscles (Ocular Motility Disorder) Panel PreventionGenetics, part of Exact Sciences United States | 14 | 14 |
|
Fibrosis of extraocular muscles, congenital type 1 (sequence analysis of KIF21A gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Neuro-ophthalmology panel. NGS panel of 38 genes. Genologica Medica Spain | 75 | 38 |
|
Fibrosis of extraocular muscles, congenital: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 5 | 4 |
|
FIBROSIS OF EXTRAOCULAR MUSCLES, TYPE 1 (CFEOM1) Laboratorio de Genetica Clinica SL Spain | 1 | 1 |
|
Fulgent Genetics United States | 1 | 1 |
|
Fulgent Genetics United States | 5130 | 4674 |
|
Intellectual Disability NGS Panel Fulgent Genetics United States | 1058 | 554 |
|
Baylor Genetics United States | 842 | 637 |
|
Comprehensive Eye Disorders NGS Panel Fulgent Genetics United States | 1018 | 459 |
|
Congenital Fibrosis of Extraocular Muscles Type Engle Laboratory Boston Children's Hospital United States | 9 | 4 |
|
Results: 1 to 15 of 15
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