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Results: 1 to 20 of 33

Tests names and labsConditionsGenes, analytes, and microbesMethods

Non-Syndromic Hearing Loss

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
11
  • S Mutation scanning of the entire coding region

Leigh’ disease

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
11
  • T Targeted variant analysis

Spinal Muscular Atrophy

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
11
  • X Mutation scanning of select exons

Sickle Cell Anemia

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
11
  • X Mutation scanning of select exons

Hemoglobin-E Disease

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
11
  • X Mutation scanning of select exons

Duchenne and Becker Muscular Dystrophy

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
21
  • X Mutation scanning of select exons

Duchenne and Becker Muscular Dystrophy

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
21
  • S Mutation scanning of the entire coding region

Leber's hereditary optic neuropathy

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
11
  • T Targeted variant analysis

Duchenne and Becker Muscular Dystrophy

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
21
  • S Mutation scanning of the entire coding region

Beta-Thalassemia

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
11
  • E Sequence analysis of select exons

Spinal Muscular Atrophy

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
11
  • C Sequence analysis of the entire coding region

Fragile-X Syndrome

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
11
  • T Targeted variant analysis

Spinal Muscular Atrophy

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
11
  • X Mutation scanning of select exons

Dentatorubral-pallidoluysian atrophy

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
11
  • T Targeted variant analysis

Hereditary haemochromatosis

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
11
  • T Targeted variant analysis

Spinocerebellar Ataxia 6

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
11
  • T Targeted variant analysis

G6PD deficiency

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
11
  • T Targeted variant analysis

Factor V deficiency

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
11
  • T Targeted variant analysis

Friedreich's ataxia

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
11
  • T Targeted variant analysis

Cystic fibrosis

Centre for cellular and molecular biology Centre for Cellular and Molecular Biology
India
11
  • X Mutation scanning of select exons

Results: 1 to 20 of 33

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.