Filters

See more specimen types...

Other countries

Results: 1 to 19 of 19 (representing 13 labs)

Tests names and labsConditionsGenes and analytesMethods

Craniofacial Sequencing Panel

Genetic Services Laboratory University of Chicago
United States
2727
  • C Sequence analysis of the entire coding region

CARPENTER SYNDROME (ACROCEPHALOPOLYSYNDACTYLY TYPE 2)

Laboratorio de Genetica Clinica SL
Spain
22
  • C Sequence analysis of the entire coding region

Carpenter Syndrome , Sequencing RAB23 Gene

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

Craniofacial Seq Analysis

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
4043
  • C Sequence analysis of the entire coding region

Craniofacial Seq + Del/Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
4043
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Craniosynostosis Seq + Del/Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
1617
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Craniosynostosis Del/Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
1617
  • D Deletion/duplication analysis

Craniofacial Del/Dup Panel

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
4043
  • D Deletion/duplication analysis

Craniosynostosis Sequence Analysis

Division of Genomic Diagnostics The Children's Hospital of Philadelphia
United States
1617
  • 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

Invitae Carpenter Syndrome Panel

Invitae
United States
22
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Craniosynostosis Panel

Invitae
United States
149
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Craniosysostosis

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
2219
  • C Sequence analysis of the entire coding region

RAB23 - Gene sequencing

Genome Diagnostics VU University Medical Center
Netherlands
11
  • E Sequence analysis of select exons
  • T Targeted variant analysis

CarrierMap

Recombine
United States
300298
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Craniosynostosis syndromes Panel

CeGaT GmbH
Germany
2020
  • C Sequence analysis of the entire coding region

Craniosynostosis (NGS panel for 30 genes)

CGC Genetics
Portugal
3130
  • C Sequence analysis of the entire coding region

RAB23

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

Carpenter syndrome (sequence analysis of RAB23 gene)

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

Results: 1 to 19 of 19

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