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Results: 1 to 20 of 242

Tests names and labsConditionsGenes and analytesMethods

TUBEROUS SCLEROSIS

Clinical Genomics Unit Hospital Universitari Germans Trias i Pujol
Spain
32
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Tuberous sclerosis

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Tuberous sclerosis

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Tuberous sclerosis-1, 191100, Autosomal dominant; TSC1 (Tuberous sclerosis complex) (MLPA)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • D Deletion/duplication analysis

Tuberous sclerosis-1, 191100, Autosomal dominant; TSC1 (Tuberous sclerosis complex) (TSC1 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

Tuberous sclerosis-1, 191100, Autosomal dominant; TSC1 (Tuberous sclerosis complex) (TSC1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

Tuberous sclerosis-1, 191100, Autosomal dominant; TSC1 (Tuberous sclerosis complex) (Prenatal) (MLPA)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • D Deletion/duplication analysis

Tuberous sclerosis-2, 613254, Autosomal dominant (Tuberous sclerosis complex) (TSC2 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

Tuberous sclerosis-2, 613254, Autosomal dominant (Tuberous sclerosis complex) (Prenatal) (MLPA)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • D Deletion/duplication analysis

Tuberous sclerosis-2, 613254, Autosomal dominant (Tuberous sclerosis complex) (TSC2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • C Sequence analysis of the entire coding region

Tuberous sclerosis-2, 613254, Autosomal dominant (Tuberous sclerosis complex) (MLPA)

Intergen Genetic Diagnosis and Research Centre
Turkey
11
  • D Deletion/duplication analysis

Tuberous Sclerosis

Asper Biogene Asper Biogene LLC
Estonia
22
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TUBEROUS SCLEROSIS

Laboratorio de Genetica Clinica SL
Spain
22
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Tuberous Sclerosis

Institute of Medical Genetics and Genomics Sir Ganga Ram Hospital
India
22
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Tuberous sclerosis

LifeLabs Genetics
Canada
11
  • C Sequence analysis of the entire coding region

Tuberous sclerosis

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Tuberous sclerosis

MedGene
Slovakia
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Tuberous sclerosis

MedGene
Slovakia
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Tuberous sclerosis

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Tuberous sclerosis

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 242

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.

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