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Results: 21 to 30 of 30

Tests names and labsConditionsGenes, analytes, and microbesMethods

IGF1R gene sequencing

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • C Sequence analysis of the entire coding region

Comprehensive Short Stature Genetic Panel

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
8260
  • C Sequence analysis of the entire coding region

Craniosynostosis NGS Panel

Fulgent Genetics
United States
33961
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

GROWTH DELAY DUE TO INSULIN-LIKE GROWTH FACTOR I RESISTANCE

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

Growth delay due to IGF-I resistance , Deletions-Duplications (MLPA) IGF1R Gene

Reference Laboratory Genetics
Spain
11
  • D Deletion/duplication analysis

Growth delay due to IGF-I resistance , Sequencing IGF1R Gene

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

IGF1R 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
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Intellectual Disability NGS Panel

Fulgent Genetics
United States
1058554
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Insulin-like growth factor I, resistance to

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

Results: 21 to 30 of 30

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.