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Results: 1 to 12 of 12

Tests names and labsConditionsGenes, analytes, and microbesMethods

Lipodystrophy, partial, acquired, susceptibility to, 608709, Autosomal dominant; APLD (Partial acquired lipodystrophy) (LMNB2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Arthrogryposis multiplex congenita, distal, type 1 Arthrogryposis, distal, type 2B Nemaline myopathy 4 CAP myopathy 2 (deletion/duplication analysis on TPM2 gene)

CGC Genetics Unilabs
Portugal
11
  • D Deletion/duplication analysis

Hypercholesterolemia panel

Genetic Services Laboratory University of Chicago
United States
1510
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dyslipidemia panel

Genetic Services Laboratory University of Chicago
United States
1729
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Lipodystrophy Panel

PreventionGenetics, part of Exact Sciences
United States
5729
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Familial Partial Lipodystrophy (FPLD) Panel

PreventionGenetics, part of Exact Sciences
United States
2916
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Lipodystrophy Panel

Genetic Services Laboratory University of Chicago
United States
1720
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

LMNB2

Institute for Human Genetics University Medical Center Freiburg
Germany
31
  • C Sequence analysis of the entire coding region

PARTIAL ACQUIRED LIPODYSTROPHY (BARRAQUER-SIMONS SYNDROME)

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

Partial acquired lipodystrophy

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

LMNB2 Single Gene

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

Clinical Exome

Fulgent Genetics
United States
51284672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 12 of 12

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