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Results: 1 to 8 of 8
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
GNAI3 - NGS including CNV analysis Centogene AG - the Rare Disease Company Germany | 1 | 1 |
|
Invitae Hypopigmentation Panel Invitae United States | 83 | 46 |
|
Invitae Facial Dysostosis and Frontonasal Dysplasia Panel Invitae United States | 44 | 28 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Auriculocondylar syndrome type 1 (sequence analysis of GNAI3 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Al Jalila Children's Genomics Center Al Jalila Childrens Speciality Hospital United Arab Emirates | 48 | 48 |
|
Auriculocondylar syndrome: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 3 | 3 |
|
Quantitative Genomic Medicine Laboratories, SL Spain | 135 | 136 |
|
Results: 1 to 8 of 8
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