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Results: 1 to 20 of 29 (representing 19 labs)

Tests names and labsConditionsGenes and analytesMethods

qCarrier Plus

Quantitative Genomic Medicine Laboratories, SL
Spain
328300
  • C Sequence analysis of the entire coding region

Oculocutaneous Albinism Type 3 (OCAIII) via the TYRP1 Gene

PreventionGenetics
United States
11
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Oculocutaneous Albinism Sequencing Panel

PreventionGenetics
United States
1613
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

TYRP1 Sequence Analysis (Prenatal Diagnosis)

Baylor Miraca Genetics Laboratories Baylor College of Medicine
United States
21
  • T Targeted variant analysis

TYRP1 Sequence Analysis (Familial Mutation/Variant Analysis)

Baylor Miraca Genetics Laboratories Baylor College of Medicine
United States
21
  • T Targeted variant analysis

TYRP1 Sequence Analysis

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

MitoMet®Plus aCGH Analysis

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

Oculocutaneous Albinism Type 3 - TYRP1 Sequencing

Children's Hospital Colorado Molecular Genetics Laboratory Children's Hospital Colorado
United States
11
  • C Sequence analysis of the entire coding region

ALBINISM: NGS PANEL

Laboratorio de Genetica Clinica SL
Spain
1313
  • C Sequence analysis of the entire coding region

OCULOCUTANEOUS ALBINISM (OCA)

Laboratorio de Genetica Clinica SL
Spain
54
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Oculocutaneous Albinism Type 3 , Sequencing TYRP1 Gene

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

Eye diseases comprehensive panel

Asper Biogene Asper Biogene LLC
Estonia
351275
  • C Sequence analysis of the entire coding region

Albinisim panel

LifeLabs Genetics
Canada
1211
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Albinism

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
1311
  • C Sequence analysis of the entire coding region

Oculocutaneous albinism type 3: TYRP1 gene sequence analysis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • C Sequence analysis of the entire coding region

Single gene testing TYRP1

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

CarrierMap

Recombine
United States
302301
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Albinism Panel

CeGaT GmbH
Germany
99
  • C Sequence analysis of the entire coding region

Albinism Panel

CeGaT GmbH
Germany
108
  • C Sequence analysis of the entire coding region

Hermansky-Pudlak Syndrome/Oculocutaneous Albinism/Pigmentation panel

Molecular Vision Laboratory
United States
4529
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 29

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.

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