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Results: 1 to 10 of 10

Tests names and labsConditionsGenes, analytes, and microbesMethods

MFRP gene mutation analysis

Genetics and Molecular Pathology SA Pathology
Australia
21
  • C Sequence analysis of the entire coding region

NHS mutation analysis

Genetics and Molecular Pathology SA Pathology
Australia
21
  • E Sequence analysis of select exons

OPA1 gene mutation analysis

Genetics and Molecular Pathology SA Pathology
Australia
51
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

TGFBI gene mutation analysis

Genetics and Molecular Pathology SA Pathology
Australia
71
  • C Sequence analysis of the entire coding region

FTL IRE mutation analysis

Genetics and Molecular Pathology SA Pathology
Australia
31
  • E Sequence analysis of select exons

PITX2 gene mutation analysis

Genetics and Molecular Pathology SA Pathology
Australia
21
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

FOXC1 gene mutation analysis

Genetics and Molecular Pathology SA Pathology
Australia
21
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

PAX6 gene mutation analysis

Genetics and Molecular Pathology SA Pathology
Australia
71
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

MYOC gene mutation analysis

Genetics and Molecular Pathology SA Pathology
Australia
11
  • C Sequence analysis of the entire coding region

CYP1B1 gene mutation analysis

Genetics and Molecular Pathology SA Pathology
Australia
31
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Results: 1 to 10 of 10

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.