U.S. flag

An official website of the United States government

Filters

See more specimen types...

Other countries

Results: 1 to 5 of 5

Tests names and labsConditionsGenes, analytes, and microbesMethods

Alopecia, neurologic defects, and endocrinopathy syndrome, 612079, Autosomal recessive (ANE syndrome) (RBM28 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Alopecia, neurologic defects, and endocrinopathy syndrome, 612079, Autosomal recessive (ANE syndrome) (RBM28 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

ANE Syndrome , Sequencing RBM28 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

RBM28 Single Gene

Fulgent Genetics
United States
11
  • 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 5 of 5

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.