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Results: 1 to 9 of 9

Tests names and labsConditionsGenes, analytes, and microbesMethods

North American Indian Childhood Cirrhosis (UTP4 Single Gene Test)

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Adams-Oliver Syndrome NGS Panel

Fulgent Genetics
United States
556
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

UTP4 Single Gene

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PIGM Single Gene

Fulgent Genetics
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

DLL4 Single Gene

Fulgent Genetics
United States
461
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

EOGT Single Gene

Fulgent Genetics
United States
461
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

GDF2 Single Gene

Fulgent Genetics
United States
331
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Hemorrhagic Telangiectasia NGS Panel

Fulgent Genetics
United States
415
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 9 of 9

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.