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Results: 1 to 11 of 11

Tests names and labsConditionsGenes, analytes, and microbesMethods

Burn-McKeown Syndrome (TXNL4A Single Gene Test)

Fulgent Genetics
United States
301
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Kaufman Oculocerebrofacial Syndrome (UBE3B Single Gene Test)

Fulgent Genetics
United States
521
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

TXNL4A Single Gene

Fulgent Genetics
United States
301
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

UBE3B Single Gene

Fulgent Genetics
United States
521
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

METTL23 Single Gene

Fulgent Genetics
United States
81
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CKAP2L Single Gene

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

CTCF Single Gene

Fulgent Genetics
United States
141
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PDGFRB Single Gene

Fulgent Genetics
United States
811
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Microcephaly NGS Panel

Fulgent Genetics
United States
32275
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 11 of 11

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.