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Results: 21 to 35 of 35

Tests names and labsConditionsGenes, analytes, and microbesMethods

Nicolaides-Baraitser syndrome

Institute of Human Genetics Cologne University
Germany
11
  • C Sequence analysis of the entire coding region

Nicolaides-Baraitser Syndrome: gene deletion/duplication

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • D Deletion/duplication analysis

Nicolaides-Baraitser Syndrome: gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

Coffin-Siris Syndrome NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
2222
  • C Sequence analysis of the entire coding region

NICOLAIDES-BARAITSER SYNDROME

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Nicolaides-Baraitser Syndrome , Sequencing SMARCA2 Gene

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

Epilepsy

Asper Biogene Asper Biogene LLC
Estonia
210204
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Epilepsy Comprehensive NGS Panel

Fulgent Genetics
United States
729398
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Cornelia de Lange and Related Disorders Panel

Genetic Services Laboratory University of Chicago
United States
1231
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nicolaides-Baraitser syndrome

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Coffin-Siris and Nicolaides-Baraitser Syndrome (CSS, NCBRS)

MGZ Medical Genetics Center
Germany
27
  • C Sequence analysis of the entire coding region

SMARCA2 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

Intellectual Disability NGS Panel

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

Coffin-Siris syndrome

Institute of Human Genetics Cologne University
Germany
97
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 21 to 35 of 35

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.