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Results: 81 to 100 of 104

Tests names and labsConditionsGenes, analytes, and microbesMethods

Axenfeld-Rieger syndrome

Department of Clinical Genetics Copenhagen University Hospital, Rigshospitalet
Denmark
57
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Primary congenital glaucoma 3A

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

Developmental Eye Disease panel

Molecular Vision Laboratory
United States
10759
  • C Sequence analysis of the entire coding region

Primary Congenital Glaucoma

Institute of Medical Genetics and Genomics Sir Ganga Ram Hospital
India
11
  • C Sequence analysis of the entire coding region

Microphthalmia-Anophthalmia-Coloboma Complex (MAC)

MGZ Medical Genetics Center
Germany
248
  • C Sequence analysis of the entire coding region

Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome

MGZ Medical Genetics Center
Germany
214
  • C Sequence analysis of the entire coding region

CYP1B1 Single Gene

Fulgent Genetics
United States
31
  • 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

Glaucoma NGS Panel

Fulgent Genetics
United States
6826
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
842637
  • D Deletion/duplication analysis

Comprehensive Eye Disorders NGS Panel

Fulgent Genetics
United States
1018459
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Glaucoma 3A, primary open angle, congenital, juvenile, or adult onset

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

Peters anomaly

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Peters anomaly

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Glaucoma 3

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Peters Anomaly

MGZ Medical Genetics Center
Germany
32
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CYP1B1-Related Primary Congenital Glaucoma

MGZ Medical Genetics Center
Germany
11
  • C Sequence analysis of the entire coding region

Primary Congenital Glaucoma

Human Developmental Genetics Laboratory Medical College of Wisconsin
United States
52
  • S Mutation scanning of the entire coding region

Glaucoma

Laboratory of Human Genetics GENOMED Health Care Center
Poland
11
  • C Sequence analysis of the entire coding region

Primay Congenital Glaucoma

Department of Clinical Genetics Copenhagen University Hospital, Rigshospitalet
Denmark
11
  • C Sequence analysis of the entire coding region

Results: 81 to 100 of 104

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.