Filters

See more specimen types...

Other countries

Results: 1 to 15 of 15 (representing 12 labs)

Tests names and labsConditionsGenes and analytesMethods

X-chromosome High Resolution microarray analysis

Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center
United States
242171
  • D Deletion/duplication analysis

X-Linked Spinal Muscular Atrophy , Sequencing UBA1 Gene

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

Neuromuscular Comprehensive Panel

Courtagen Diagnostics Laboratory Courtagen Life Sciences
United States
454305
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Atypical Spinal Muscular Atrophy Advanced Sequencing Evaluation

Athena Diagnostics Inc
United States
1010
  • C Sequence analysis of the entire coding region

Invitae Hereditary Motor Neuropathy Panel

Invitae
United States
2422
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Comprehensive Neuropathies Panel

Invitae
United States
10070
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Spinal muscular atrophy, X-linked infantile: UBA1 gene sequence analysis (exon 15)

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
11
  • E Sequence analysis of select exons

Spinal Muscular Atrophy (SMA) Panel

CeGaT GmbH
Germany
4427
  • C Sequence analysis of the entire coding region

Spinal Muscular Atrophy Panel

CeGaT GmbH
Germany
1127
  • C Sequence analysis of the entire coding region

Hereditary Spastic Paraplegias (HSP) and differential diagnoses Panel

CeGaT GmbH
Germany
147143
  • C Sequence analysis of the entire coding region

UBA1

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

X-Linked Spinal Muscular Atrophy (XLSMA) - UBE1 DNA Sequencing Test

Athena Diagnostics Inc
United States
11
  • E Sequence analysis of select exons

Spinal muscular atrophy, X-linked, infantile (SMAX2, sequence analysis of UBA1 gene)

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

Spinal Muscular Atrophy, X-Linked Infantile

Medizinisch Genetisches Zentrum München MGZ München
Germany
11
  • C Sequence analysis of the entire coding region

Spinal muscular atrophy, X-linked infantile

Institute of Human Genetics Cologne University
Germany
11
  • C Sequence analysis of the entire coding region

Results: 1 to 15 of 15

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