Filters

See more specimen types...

Other countries

Results: 1 to 20 of 21 (representing 11 labs)

Tests names and labsConditionsGenes and analytesMethods

OTX2 Sequence Analysis

Baylor Miraca Genetics Laboratories
United States
21
  • C Sequence analysis of the entire coding region

OTX2 Prenatal Sequence Analysis

Baylor Miraca Genetics Laboratories
United States
21
  • E Sequence analysis of select exons

OTX2 Familial Mutation/Variant Analysis

Baylor Miraca Genetics Laboratories
United States
21
  • E Sequence analysis of select exons

Leber Congential Amaurosis Panel (MitomeNGS)

Baylor Miraca Genetics Laboratories
United States
3219
  • C Sequence analysis of the entire coding region

MitoMet®Plus aCGH Analysis

Baylor Miraca Genetics Laboratories
United States
845637
  • D Deletion/duplication analysis

Septo-optic dysplasia

Molecular Vision Laboratory
United States
124
  • C Sequence analysis of the entire coding region

OTX2 Gene Sequencing

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
31
  • C Sequence analysis of the entire coding region

Septooptic dysplasia

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
119
  • C Sequence analysis of the entire coding region

Combined Pituitary Hormone Deficiency NGS Panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
76
  • C Sequence analysis of the entire coding region

Isolated Growth Hormone Deficiency NGS Panel

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
1410
  • C Sequence analysis of the entire coding region

Single gene testing OTX2

CeGaT GmbH
Germany
21
  • C Sequence analysis of the entire coding region

Developmental Eye Disease panel

Molecular Vision Laboratory
United States
10959
  • C Sequence analysis of the entire coding region

OTX2

Medizinisch Genetisches Zentrum München MGZ München
Germany
31
  • C Sequence analysis of the entire coding region

OTX2

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Pituitary hormone deficiency, combined 6 (sequence analysis of OTX2 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Leber Congenital Amaurosis: Sequencing and Deletion/Duplication Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
3218
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Eye Disorders: Comprehensive Sequencing and Deletion/Duplication Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
320207
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Anophthalmia/Microphthalmia/Anterior Segment Dysgenesis/Anomaly: Sequencing Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
4023
  • C Sequence analysis of the entire coding region

Septo-optic Dysplasia NGS Panel

Fulgent Genetics
United States
135
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

OTX2 mutation analysis

DNA Diagnostics Laboratory Academic Medical Centre, University of Amsterdam
Netherlands
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 21

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.

Support Center