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Results: 41 to 57 of 57

Tests names and labsConditionsGenes, analytes, and microbesMethods

Familial Lipoprotein Lipase Deficiency: gene deletion/duplication

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • D Deletion/duplication analysis

Familial Lipoprotein Lipase Deficiency: gene sequencing

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
11
  • C Sequence analysis of the entire coding region

Familial Lipoprotein Lipase Deficiency

Asper Biogene Asper Biogene LLC
Estonia
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypertriglyceridemia

Asper Biogene Asper Biogene LLC
Estonia
86
  • C Sequence analysis of the entire coding region

MAJOR HYPERTRIGLYCERIDEMIA

Laboratorio de Genetica Clinica SL
Spain
56
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HYPERLIPOPROTEINEMIA TYPE 1

Laboratorio de Genetica Clinica SL
Spain
44
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Familial lipoprotein lipase deficiency

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

Familial lipoprotein lipase deficiency

Bioarray
Spain
11
  • D Deletion/duplication analysis

LPL

Institute of Human Genetics Medical University Innsbruck
Austria
21
  • S Mutation scanning of the entire coding region

LPL Sequencing

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
21
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

LPL Single Gene

Fulgent Genetics
United States
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

APOA5

Department of Endocrinology and Metabolism Okinaka Memorial Institute for Medical Research
Japan
11
  • S Mutation scanning of the entire coding region

LPL

Department of Endocrinology and Metabolism Okinaka Memorial Institute for Medical Research
Japan
11
  • S Mutation scanning of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypertriglyceridaemia genetic screen

Cardiovascular Genetics Laboratory PathWest Laboratory Medicine WA - Fiona Stanley Hospital
Australia
27
  • C Sequence analysis of the entire coding region

Hyperlipoproteinemia, type I

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

LPL deficiency

Department of Endocrinology and Metabolism Okinaka Memorial Institute for Medical Research
Japan
11
  • C Sequence analysis of the entire coding region

Results: 41 to 57 of 57

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.