U.S. flag

An official website of the United States government

Filters

See more specimen types...

Other countries

See more countries

Results: 21 to 40 of 50

Tests names and labsConditionsGenes, analytes, and microbesMethods

Multiple Epiphyseal Dysplasia via the MATN3 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

Skeletal Disorders Panel

Baylor Genetics
United States
1354
  • C Sequence analysis of the entire coding region

Bone diseases panel_v.2.0

CGC Genetics Unilabs
Portugal
1662
  • C Sequence analysis of the entire coding region

Skeletal Diseases Panel

Mendelics
Brazil
1333
  • C Sequence analysis of the entire coding region

SHORT STATURE EXOME PANEL

Laboratorio de Genetica Clinica SL
Spain
1152
  • E Sequence analysis of select exons

SKELETAL DYSPLASIAS PANEL

Laboratorio de Genetica Clinica SL
Spain
1643
  • E Sequence analysis of select exons

Spondylometaphyseal / spondyloepimetaphyseal dysplasia panel. 28-gene NGS panel.

Genologica Medica
Spain
6928
  • C Sequence analysis of the entire coding region

Central skeletal dysplasias panel. NGS panel of 111 genes.

Genologica Medica
Spain
258111
  • C Sequence analysis of the entire coding region

Genomic Unity® Custom Analysis

Variantyx, Inc.
United States
14054
  • D Deletion/duplication analysis
  • X Mutation scanning of select exons
  • C Sequence analysis of the entire coding region

Epiphyseal dysplasia, multiple: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
77
  • C Sequence analysis of the entire coding region

Comprehensive Growth Disorders / Skeletal Dysplasias and Disorders Panel

Blueprint Genetics
Finland
2308
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Skeletal Dysplasias and Disorders Panel

Blueprint Genetics
Finland
1246
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasias Core Panel

Blueprint Genetics
Finland
1111
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

EPIPHYSEAL DYSPLASIA, MULTIPLE (AUTOSOMAL DOMINANT)

Laboratorio de Genetica Clinica SL
Spain
15
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Spondylometaphyseal / Spondyloepi-(meta)-physeal Dysplasia Panel

Blueprint Genetics
Finland
228
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Multiple epiphyseal dysplasia and pseudoachondroplasia Panel

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

Spondylometaphyseal dysplasia and Spondylo-epi-(meta)-physeal dysplasia Panel

CeGaT GmbH
Germany
2727
  • C Sequence analysis of the entire coding region

Multiple epiphyseal dysplasia type 1

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

Multiple epiphyseal dysplasia type 5

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

Single gene testing MATN3

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

Results: 21 to 40 of 50

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.