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Results: 1 to 20 of 29 (representing 18 labs)

Tests names and labsConditionsGenes and analytesMethods

Robinow syndrome, autosomal recessive - 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 recessive (RRS) - Deletion/Duplication

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

Robinow syndrome, autosomal recessive (RRS) - 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

ROR2 deletion/duplication analysis

Genetic Services Laboratory University of Chicago
United States
21
  • D Deletion/duplication analysis

ROR2 sequencing

Genetic Services Laboratory University of Chicago
United States
21
  • C Sequence analysis of the entire coding region

ROR2. MLPA testing

Instituto de Medicina Genomica
Spain
11
  • D Deletion/duplication analysis

ROR2. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

WNT5A. Complete sequencing

Instituto de Medicina Genomica
Spain
11
  • C Sequence analysis of the entire coding region

Skeletal Dysplasia Panel

Insight Medical Genetics
United States
278
  • X Mutation scanning of select exons

Robinow Syndrome and Autosomal Recessive Brachydactyly, Type B1 via the ROR2 Gene

PreventionGenetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Robinow Syndrome , Deletions-Duplications (MLPA) ROR2 Gene

Reference Laboratory Genetics
Spain
11
  • D Deletion/duplication analysis

Robinow Syndrome, Sequencing ROR2 Gene

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

Abnormal/Ambiguous Genitalia Sequencing Panel

Genetic Services Laboratory University of Chicago
United States
8272
  • 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, AR (sequence analysis of ROR2 gene)

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

ROR2

Fulgent Genetics
United States
21
  • 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

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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