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Results: 1 to 20 of 28 (representing 17 labs)

Tests names and labsConditionsGenes and analytesMethods

Parkes Weber syndrome

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

Parkes Weber syndrome - Sanger / Del Dup Comprehensive

Connective Tissue Gene Tests
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Parkes Weber syndrome (PKWS) - Deletion/Duplication

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

Parkes Weber syndrome (PKWS) - Sanger Sequencing

Connective Tissue Gene Tests
United States
11
  • C Sequence analysis of the entire coding region

RASA1-only analysis

Medical Genomics Laboratory Department of Genetics UAB
United States
21
  • D Deletion/duplication analysis

RASA1-Related Disorders (RASA1) Sequencing and Deletion/Duplication

ARUP Laboratories, Molecular Genetics and Genomics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

RASA1. Complete sequencing

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

Vascular Malformations Panel, Sequencing and Deletion/Duplication, 14 Genes

ARUP Laboratories, Molecular Genetics and Genomics
United States
1114
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Parkes Weber syndrome (sequence analysis of RASA1 gene)

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

Parkes Weber syndrome (sequence analysis of RASA1 gene)

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

PARKES-WEBER SYNDROME

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

Parkes-Weber Syndrome, Sequencing RASA1 Gene

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

Invitae Hereditary Hemorrhagic Telangiectasia Panel

Invitae
United States
64
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Capillary Malformation-Arteriovenous Malformation Syndrome Test

Invitae
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Parkes Weber syndrome

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

RASopathies Panel

CeGaT GmbH
Germany
2323
  • C Sequence analysis of the entire coding region

RASopathies Panel

CeGaT GmbH
Germany
2323
  • C Sequence analysis of the entire coding region

RASopathies Panel

CeGaT GmbH
Germany
2323
  • C Sequence analysis of the entire coding region

RASA1

Fulgent Genetics
United States
31
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Hemorrhagic Telangiectasia (HHT) Panel, Sequencing Deletion/Duplication, 5 Genes

ARUP Laboratories, Molecular Genetics and Genomics
United States
75
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 28

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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