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Results: 1 to 16 of 16 (representing 13 labs)

Tests names and labsConditionsGenes and analytesMethods

Skeletal Disorders and Joint Problems Sequencing Panel

PreventionGenetics
United States
327258
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Symphalangism, Proximal, Multiple Synostoses Syndrome, Stapes Ankylosis with Broad Thumb and Toes, Tarsal-Carpal Coalition Syndrome, and Brachydactyly, Type B2 via the NOG Gene

PreventionGenetics
United States
51
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

BRACHYDACTYLY TYPE B2

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Brachydactyly Type B2, Sequencing NOG Gene

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

qGenEx Craniofacial Anomalies

Quantitative Genomic Medicine Laboratories, SL
Spain
135136
  • C Sequence analysis of the entire coding region

Brachydactyly type B2: NOG gene sequence analysis

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

Isolated limb hypoplasia and limb reduction defects: Split-hand/foot; Synostosis; isolated Brachydactyly; Polydactyly; Syndactyly Panel

CeGaT GmbH
Germany
1920
  • C Sequence analysis of the entire coding region

Brachydactyly, type B2

Bioarray
Spain
11
  • D Deletion/duplication analysis

NOG

Fulgent Genetics
United States
51
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasias NGS panel

Fulgent Genetics
United States
370161
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasia: Sequencing Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
364163
  • C Sequence analysis of the entire coding region

Limb Malformation: Sequencing Panel

EGL Genetic Diagnostics Eurofins Clinical Diagnostics
United States
12146
  • C Sequence analysis of the entire coding region

Brachydactyly B2

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Brachydactyly B2

Praxis fuer Humangenetik Wien
Austria
11
  • C Sequence analysis of the entire coding region

Brachydactyly B2

Praxis fuer Humangenetik Wien
Austria
11
  • S Mutation scanning of the entire coding region

Brachydactyly, Type B2

Michigan Medical Genetics Laboratories University of Michigan
United States
51
  • C Sequence analysis of the entire coding region

Results: 1 to 16 of 16

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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