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Results: 481 to 497 of 497

Tests names and labsConditionsGenes, analytes, and microbesMethods

Clinical Exome

Fulgent Genetics
United States
51304674
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Noonan Spectrum Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
4231
  • 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

Comprehensive Cardiovascular NGS Panel

Fulgent Genetics
United States
696250
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Watson syndrome

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neurofibromatosis I

Praxis fuer Humangenetik Wien
Austria
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypertrophic Cardiomyopathy Panel

Cincinnati Children's Hospital Medical Center Genetics and Genomics Diagnostic Laboratory Cincinnati Children's Hospital Medical Center
United States
13198
  • C Sequence analysis of the entire coding region

Hereditary onco-endocrino tumors (50 genes)

Center for Human Genetics Cliniques Universitaires Saint Luc
Belgium
2549
  • C Sequence analysis of the entire coding region

Hereditary Neuroendocrine Tumor Disorder

Genetics Laboratory University of Oklahoma Health Sciences Center
United States
15
  • C Sequence analysis of the entire coding region

Neurofibromatosis 1 (NF1)

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neurofibromatosis 1

Institute of Medical Genetics and Genomics Sir Ganga Ram Hospital
India
11
  • L Linkage analysis
  • T Targeted variant analysis

Neurofibromatosis type I (von Recklinghausen`s Disease)

Laboratory of Human Genetics GENOMED Health Care Center
Poland
11
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons
  • C Sequence analysis of the entire coding region

Noonan spectrum

Genetics Laboratory University of Oklahoma Health Sciences Center
United States
117
  • C Sequence analysis of the entire coding region

Neurofibromatosis-Noonan syndrome

Center for Human Genetics, Inc
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neurofibromatosis

Genetics Laboratory University of Oklahoma Health Sciences Center
United States
12
  • C Sequence analysis of the entire coding region

Hereditary Endocrine Cancer

Genetics Laboratory University of Oklahoma Health Sciences Center
United States
122
  • C Sequence analysis of the entire coding region

Neurofibromatosis Syndrome Type 1

Center for Human Genetics, Inc
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 481 to 497 of 497

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.