Filters
Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
---|---|---|---|
PCDH19 Sequence Analysis (Familial Mutation/Variant Analysis) Baylor Genetics United States | 1 | 1 |
|
Baylor Genetics United States | 1 | 1 |
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X-chromosome High Resolution microarray analysis Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center United States | 240 | 171 |
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Genetic Services Laboratory University of Chicago United States | 21 | 28 |
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Early Infantile Epileptic Encephalopathy Panel Genetic Services Laboratory University of Chicago United States | 47 | 125 |
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MNG Laboratories (Medical Neurogenetics, LLC.) United States | 414 | 800 |
|
MNG Laboratories (Medical Neurogenetics, LLC.) United States | 54 | 45 |
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Cortical Malformations and Epilepsy Panel with interpretation Clinical Genomics Laboratory Washington University in St. Louis United States | 35 | 39 |
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Comprehensive Epilepsy Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States | 234 | 240 |
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Developmental and epileptic encephalopathy: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 91 | 90 |
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Intellectual Disability X-linked Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 136 | 90 |
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CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 35 | 17 |
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Intellectual Disability & Autism Spectrum Disorders Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 210 | 139 |
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Rett & Angelman Syndrome Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 38 | 21 |
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CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 44 | 21 |
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CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 132 | 83 |
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Angelman/Rett-like syndrome panel Al Jalila Children’s Genomics Center Al Jalila Childrens Speciality Hospital United Arab Emirates | 19 | 19 |
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Epileptic encephalopathy, early infantile: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 76 | 76 |
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Fulgent Genetics United States | 354 | 209 |
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Fulgent Genetics United States | 78 | 23 |
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