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Results: 61 to 77 of 77

Tests names and labsConditionsGenes, analytes, and microbesMethods

Bardet-Biedl Syndrome: gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
2323
  • C Sequence analysis of the entire coding region

Bardet-Biedl Syndrome NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
2426
  • C Sequence analysis of the entire coding region

BARDET-BIEDL SYNDROME

Laboratorio de Genetica Clinica SL
Spain
1214
  • C Sequence analysis of the entire coding region

BARDET-BIEDL SYNDROME (NGS)

Laboratorio de Genetica Clinica SL
Spain
1723
  • C Sequence analysis of the entire coding region

Senior-Loken Syndrome panel

Molecular Vision Laboratory
United States
104
  • C Sequence analysis of the entire coding region

Joubert Syndrome Panel

Molecular Vision Laboratory
United States
4824
  • C Sequence analysis of the entire coding region

Invitae Congenital Heart Defects and Heterotaxy Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
12882
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Leber congenital amaurosis panel

Molecular Vision Laboratory
United States
4323
  • C Sequence analysis of the entire coding region

Bardet-Biedl syndrome panel

Molecular Vision Laboratory
United States
3823
  • C Sequence analysis of the entire coding region

Retinal Dystrophy Panel

Molecular Vision Laboratory
United States
372283
  • C Sequence analysis of the entire coding region

Bardet-Biedl Syndrome Panel

CeGaT GmbH
Germany
1724
  • C Sequence analysis of the entire coding region

Ataxia and differential diagnoses Panel

CeGaT GmbH
Germany
173204
  • C Sequence analysis of the entire coding region

Bardet Biedl Syndrome Panel

CeGaT GmbH
Germany
1724
  • C Sequence analysis of the entire coding region

Bardet Biedl Syndrome Panel

CeGaT GmbH
Germany
1724
  • C Sequence analysis of the entire coding region

Invitae Ciliopathies Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
144102
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Bardet-Biedl Syndrome Panel

Labcorp Genetics (formerly Invitae) LabCorp
United States
1916
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bardet-Biedl syndrome 14

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • C Sequence analysis of the entire coding region

Results: 61 to 77 of 77

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.