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Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
Baylor Genetics United States | 842 | 637 |
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Panel of premature ovarian failure. NGS panel of 15 genes. Genologica Medica Spain | 50 | 15 |
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FOXL2 Sequencing and Deletion/Duplication Analysis DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children United States | 1 | 1 |
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Fulgent Genetics United States | 92 | 56 |
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Fulgent Genetics United States | 76 | 41 |
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Microphthalmia, Anophthalmia, and Coloboma Panel NGS Panel Fulgent Genetics United States | 244 | 78 |
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Blepharophimosis, Ptosis, and Epicanthus Inversus: gene deletion/duplication CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 | 1 |
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Blepharophimosis, Ptosis, and Epicanthus Inversus: gene sequencing CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 1 | 1 |
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BPES SYNDROME (BLEPHAROPHIMOSIS-PTOSIS-EPICANTHUS INVERSUS) Laboratorio de Genetica Clinica SL Spain | 1 | 1 |
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Blepharophimosis-Ptosis-Epicanthus Inversus , Deletions-Duplications (MLPA) FOXL2 Gene Reference Laboratory Genetics Spain | 1 | 1 |
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Blepharophimosis-Ptosis-Epicanthus Inversus, Sequencing FOXL2 Gene Reference Laboratory Genetics Spain | 1 | 1 |
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Fulgent Genetics United States | 3 | 1 |
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Blepharophimosis, epicanthus inversus, and ptosis: FOXL2 gene deletions-duplications analysis (MLPA) GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Spain | 1 | 1 |
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Blepharophimosis - epicanthus inversus - ptosis Bioarray Spain | 1 | 1 |
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Fulgent Genetics United States | 2 | 1 |
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Fulgent Genetics United States | 5129 | 4672 |
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Comprehensive Eye Disorders NGS Panel Fulgent Genetics United States | 1018 | 459 |
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Blepharophimosis, epicanthus inversus, and ptosis: FOXL2 gene sequence analysis GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases Spain | 1 | 1 |
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Blephrophemosis-Ptosis-Epicanthosis syndrome - FOXL2 Deletion/Duplication Analysis Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 1 | 1 |
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Blephrophemosis-Ptosis-Epicanthosis syndrome - FOXL2 Sequence Analysis Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 1 | 1 |
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IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.