U.S. flag

An official website of the United States government

Filters

Other countries

Results: 1 to 5 of 5

Tests names and labsConditionsGenes, analytes, and microbesMethods

Invitae Microcephalic Primordial Dwarfism and Seckel Syndrome Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
4838
  • D Deletion/duplication analysis

Invitae Skeletal Disorders Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
624349
  • D Deletion/duplication analysis

Seckel syndrome 10, 617253, Autosomal recessive; SCKL10 (Microcephalic primordial dwarfism-insulin resistance syndrome) (NSMCE2 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

Seckel syndrome 10, 617253, Autosomal recessive; SCKL10 (Microcephalic primordial dwarfism-insulin resistance syndrome) (NSMCE2 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

Seckel syndrome: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
99
  • 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.