Filters

See more specimen types...

Other countries

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

Tests names and labsConditionsGenes and analytesMethods

Rapid microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • H Detection of homozygosity
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Ulnar-Mammary syndrome

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

TBX3. Complete sequencing

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

Ulnar-Mammary Syndrome via the TBX3 Gene

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

Selected Genetic Syndromes with skeletal involvement Panel

CeGaT GmbH
Germany
3642
  • C Sequence analysis of the entire coding region

Ulnar-mammary syndrome

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

Congenital Heart Defects Panel

CeGaT GmbH
Germany
4244
  • C Sequence analysis of the entire coding region

qChip

Quantitative Genomic Medicine Laboratories, SL
Spain
184162
  • D Deletion/duplication analysis

Ulnar-mammary syndrome (sequence analysis of TBX3 gene)

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

TBX3

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
370161
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasia: Sequencing Panel

Emory Genetics Laboratory Emory University School of Medicine
United States
364163
  • C Sequence analysis of the entire coding region

Limb Malformation: Sequencing Panel

Emory Genetics Laboratory Emory University School of Medicine
United States
12146
  • C Sequence analysis of the entire coding region

Ulnar-Mammary Syndrom

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

Ulnar-Mammary Syndrom

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

Ulnar-Mammary Syndrome

Bioscientia GmbH Center for Human Genetics
Germany
11
  • 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.

Support Center