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Results: 61 to 80 of 91

Tests names and labsConditionsGenes, analytes, and microbesMethods

Noonan Spectrum Disorders Panel, Sequencing, Fetal

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
1015
  • C Sequence analysis of the entire coding region

NEUROFIBROMATOSIS 1-LIKE SYNDROME (LEGIUS SYNDROME)

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

LEGIUS SYNDROME (NEUROFIBROMATOSIS TYPE 1-LIKE)

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

Invitae Overgrowth and Macrocephaly Syndromes Panel

Invitae
United States
4320
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Noonan Spectrum Disorders Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
2421
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Legius syndrome

Labor Dr. Wisplinghoff
Germany
11
  • C Sequence analysis of the entire coding region

Epilepsy Comprehensive NGS Panel

Fulgent Genetics
United States
729398
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

SPRED1 Gene Sequencing and Deletion/Duplication Analysis

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Legius syndrome

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

Single gene testing SPRED1

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

RASopathy NGS Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
723
  • C Sequence analysis of the entire coding region

RASopathies Panel

CeGaT GmbH
Germany
2323
  • C Sequence analysis of the entire coding region

RASopathies Panel

CeGaT GmbH
Germany
2323
  • C Sequence analysis of the entire coding region

RASopathies Panel

CeGaT GmbH
Germany
2323
  • C Sequence analysis of the entire coding region

Genetic disorders with abnormal pigmentation Panel

CeGaT GmbH
Germany
2932
  • C Sequence analysis of the entire coding region

Disorders associated with malignancy Panel

CeGaT GmbH
Germany
2645
  • C Sequence analysis of the entire coding region

SPRED1 Single Gene

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

Hypertrophic Cardiomyopathy NGS Panel

Fulgent Genetics
United States
37586
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Legius Syndrome Test

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

Neurofibromatosis NGS Panel

Fulgent Genetics
United States
93
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 61 to 80 of 91

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.