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Results: 41 to 60 of 95

Tests names and labsConditionsGenes, analytes, and microbesMethods

MitoMet®Plus aCGH Analysis

Baylor Genetics
United States
842637
  • D Deletion/duplication analysis

Galactosemia Mutation Analysis

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
11
  • T Targeted variant analysis

Galactosemia Type I (Classic and Variant Galactosemia) via the GALT Gene

PreventionGenetics, part of Exact Sciences
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

GALT

Institute for Human Genetics University Medical Center Freiburg
Germany
11
  • C Sequence analysis of the entire coding region

GALACTOSEMIA

BioReference Health
United States
11
  • T Targeted variant analysis

Inherited Metabolic Disorders Panel

Dhiti Omics Technologies Private Ltd
India
376317
  • C Sequence analysis of the entire coding region

Cataract panel. NGS panel of 69 genes.

Genologica Medica
Spain
14669
  • C Sequence analysis of the entire coding region

Metabolic liver failure panel. 16-gene NGS panel.

Genologica Medica
Spain
1916
  • C Sequence analysis of the entire coding region

Galactosemia panel

Genologica Medica
Spain
33
  • C Sequence analysis of the entire coding region

Mono and Disaccharide Congenital Disorders Panel. 9-gene NGS panel.

Genologica Medica
Spain
149
  • C Sequence analysis of the entire coding region

Galactosemia panel

Genologica Medica
Spain
33
  • C Sequence analysis of the entire coding region

Panel of premature ovarian failure. NGS panel of 15 genes.

Genologica Medica
Spain
5015
  • C Sequence analysis of the entire coding region

Galactosemia I

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

GALT Gene Sequencing

Lifecell International Pvt. Ltd
India
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Extended Carrier Screening

HNL Genomics Connective Tissue Gene Tests
United States
4445
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

GALT Prenatal Sequence Analysis (GeneAware) (Prenatal Sequence Analysis)

Baylor Genetics
United States
11
  • E Sequence analysis of select exons

Super Panel Plus

NxGen MDx
United States
116117
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Super Panel 113

NxGen MDx
United States
113115
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Foresight

Myriad Genetics, Inc.
United States
112110
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Galactosemia

Al Jalila Children's Genomics Center Al Jalila Childrens Speciality Hospital
United Arab Emirates
43
  • C Sequence analysis of the entire coding region

Results: 41 to 60 of 95

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.