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Waardenburg syndrome (deletion/duplication analysis of TYR gene)
TYR
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When it is not possible to collect the minimum volume for the test, please contact CGC Genetics
2
Maximum shipping time to ensure sample quality
Turnaround Time (Days)
- 30
Specialties
- Dermatology, Rare diseases, Neurology / Neuropediatrics, Otorhinolaryngology, Pediatrics, Dysmorphology
CGC Reference
- 4985
Associated Tests
Albinism oculocutaneous (deletion/duplication analysis on OCA2 and TYR genes)
Albinism, oculocutaneous type I (sequence analysis of TYR gene)
Waardenburg syndrome (NGS panel of 7 genes)
Albinism (NGS panel of 12 genes)
Hermansky-Pudlak syndrome and differential diagnosis (WES based NGS panel for 17 genes, including CNV analysis)