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Results: 1 to 4 of 4

Tests names and labsConditionsGenes, analytes, and microbesMethods

Velocardiofacial syndrome, 192430, Autosomal dominant (22q11.2 deletion syndrome) (FISH)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • F Fluorescence in situ hybridization (FISH)

Velocardiofacial syndrome, 192430, Autosomal dominant (22q11.2 deletion syndrome) (Prenatal) (FISH)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • F Fluorescence in situ hybridization (FISH)

Microarray Testing

Cytogenetics Laboratory SUNY Upstate Medical University
United States
1141
  • F Fluorescence in situ hybridization (FISH)

Chromosome FISH

Cytogenomics Laboratory Johns Hopkins Hospital
United States
32
  • F Fluorescence in situ hybridization (FISH)

Results: 1 to 4 of 4

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.