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Results: 1 to 20 of 20 (representing 13 labs)

Tests names and labsConditionsGenes and analytesMethods

WNT5A deletion/duplication analysis

Genetic Services Laboratory University of Chicago
United States
11
  • D Deletion/duplication analysis

WNT5A sequencing

Genetic Services Laboratory University of Chicago
United States
11
  • C Sequence analysis of the entire coding region

Robinow syndrome, autosomal dominant 1 - Sanger / Del Dup Comprehensive

Connective Tissue Gene Tests
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Robinow syndrome, autosomal dominant 1 (DRS1) - Deletion/Duplication

Connective Tissue Gene Tests
United States
11
  • D Deletion/duplication analysis

Robinow syndrome, autosomal dominant (DRS) - Sanger Sequencing

Connective Tissue Gene Tests
United States
11
  • C Sequence analysis of the entire coding region

Robinow syndrome

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Robinow Syndrome, Sequencing WNT5A Gene

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

Comprehensive Skeletal / Malformation Syndrome Panel

Blueprint Genetics
Finland
13429
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Micromelic Dysplasia Panel

Blueprint Genetics
Finland
624
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

DVL1

Fulgent Genetics
United States
711
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Micromelic dysplasia: acromelic, acromesomelic, mesomelic and rhizo-mesomelic dysplasia Panel

CeGaT GmbH
Germany
1819
  • C Sequence analysis of the entire coding region

Cornelia de Lange Syndrome PLUS Sequencing Panel

Genetic Services Laboratory University of Chicago
United States
1121
  • C Sequence analysis of the entire coding region

Robinow syndrome

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

Robinow syndrome (sequence analysis of WNT5A gene)

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

WNT5A

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasias NGS panel

Fulgent Genetics
United States
369161
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasia

Asper Biotech Asper Biotech Ltd.
Estonia
2510
  • C Sequence analysis of the entire coding region

Skeletal Dysplasia: Sequencing Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
363163
  • C Sequence analysis of the entire coding region

Disproportionate Short Stature: Sequencing Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
19877
  • C Sequence analysis of the entire coding region

Robinow syndrome: WNT5A gene sequence analysis

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

Results: 1 to 20 of 20

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