GTR Home > Tests > Search results - Acrocephalosyndactyly type I

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Your search term can be found in tests with a total of 2340 conditions. Only 1000 conditions are displayed in this filter box. Please type the name of the condition in the search box in this filter to find the specific condition. You can use the filters below to narrow down your results.
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GTR test search results for C0001193[DISCUI]

C Clinical test, R Research test

Showing 1 to 20 of 34 tests for 1 condition in 20 labs

CApert syndrome

Lab: Centogene AG - the Rare Disease Company Rostock, Mecklenburg-Vorpommern, Germany
Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

CApert syndrome - Sanger Sequencing

Lab: Connective Tissue Gene Tests Allentown, Pennsylvania, United States
Test targets
Methods
  • C Sequence analysis of the entire coding region

CApert syndrome - Sanger Sequencing

Lab: Connective Tissue Gene Tests Allentown, Pennsylvania, United States
Test targets
Methods
  • C Sequence analysis of the entire coding region

CFacial Dysostosis Related Disorders NextGen Sequencing (NGS) Panel

Lab: PreventionGenetics Marshfield, Wisconsin, United States
Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis
Total conditions (33)
Total targets (19)

CCraniosynostosis and Related Disorders NextGen Sequencing (NGS) Panel

Lab: PreventionGenetics Marshfield, Wisconsin, United States
Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis
Total conditions (19)
Total targets (5)

CApert Syndrome, Crouzon Syndrome, Pfeiffer Syndrome

Lab: Human Genetics University Hospital Bern Berne, Bern, Switzerland
Test targets
Methods
  • C Sequence analysis of the entire coding region

CTruGenome Predisposition Screen (Whole Genome Sequencing)

Lab: Illumina Clinical Services Laboratory Illumina San Diego, California, United States
Test targets
Methods
  • C Sequence analysis of the entire coding region
Total conditions (1541)
Total targets (1578)

CFGFR2, COMP, COL11A1, COL11A2, EVC, TRIP11, EVC2. NextGeneDx.Complete sequencing by NGS

Lab: Instituto de Medicina Genomica Paterna, Comunidad Valenciana, Spain
Test targets
Methods
  • C Sequence analysis of the entire coding region
Total conditions (20)
Total targets (7)

CFGFR2-Related Disorders via the FGFR2 Gene

Lab: PreventionGenetics Marshfield, Wisconsin, United States
Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis
Total conditions (8)

CCraniosynostosis

Test targets
Methods
  • C Sequence analysis of the entire coding region
Total conditions (13)

CApert syndrome

Lab: Bioarray Elche, Comunidad Valenciana, Spain
Test targets
Methods
  • C Sequence analysis of the entire coding region

CApert syndrome (sequence analysis of FGFR2 gene)

Lab: CGC Genetics Porto, Porto, Portugal
Test targets
Methods
  • C Sequence analysis of the entire coding region

CSingle gene testing FGFR2

Lab: CeGaT GmbH Tuebingen, Baden-Wurttemberg, Germany
Total conditions (11)

CFGFR2

Lab: Fulgent Clinical Diagnostics Lab Fulgent Diagnostics Temple City, California, United States
Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
Total conditions (11)

CSkeletal Dysplasias NGS panel

Lab: Fulgent Clinical Diagnostics Lab Fulgent Diagnostics Temple City, California, United States
Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
Total conditions (371)
Total targets (161)

CFGFR-Related Craniosynostosis NGS Panel

Lab: Fulgent Clinical Diagnostics Lab Fulgent Diagnostics Temple City, California, United States
Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
Total conditions (25)

CCraniosynostosis NGS Panel

Lab: Transgenomic New Haven, Connecticut, United States
Test targets
Methods
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
Total conditions (17)

CSkeletal Dysplasia

Lab: Asper Biotech Asper Biotech Ltd. Tartu, Tartumaa, Estonia
Test targets
Methods
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis
Total conditions (25)
Total targets (10)

CSkeletal Dysplasia: Sequencing Panel

Test targets
Methods
  • C Sequence analysis of the entire coding region
Total conditions (365)
Total targets (163)

Showing 1 to 20 of 34 tests for 1 condition in 20 labs

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