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Results: 61 to 80 of 95

Tests names and labsConditionsGenes, analytes, and microbesMethods

Multiple Endocrine Neoplasia Type 2, Deletions-Duplications (MLPA) RET Gene

Reference Laboratory Genetics
Spain
21
  • D Deletion/duplication analysis

Multiple Endocrine Neoplasia Type 2B, Sequencing Exons (15,16) RET Gene

Reference Laboratory Genetics
Spain
11
  • E Sequence analysis of select exons

Comprehensive Hereditary Cancer Panel

Baylor Genetics
United States
13261
  • E Sequence analysis of select exons

Hereditary Endocrine Cancer Panel

Baylor Genetics
United States
5115
  • E Sequence analysis of select exons

Hereditary Paraganglioma/Pheochromocytoma Panel

Baylor Genetics
United States
219
  • D Deletion/duplication analysis
  • E Sequence analysis of select exons

Endocrine tumours

Institute of Human Genetics Cologne University
Germany
1711
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Multiple endocrine neoplasia, type 2

Labor Dr. Wisplinghoff
Germany
21
  • C Sequence analysis of the entire coding region

Waardenburg Syndrome panel

Molecular Vision Laboratory
United States
197
  • C Sequence analysis of the entire coding region

Invitae Pediatric Solid Tumors Panel

Invitae
United States
9048
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Paraganglioma-Pheochromocytoma Comprehensive Panel

Fulgent Genetics
United States
2911
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Full Comprehensive Cancer Panel

Fulgent Genetics
United States
329127
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Thyroid Cancer Comprehensive Panel

Fulgent Genetics
United States
377
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Comprehensive Hereditary Cancer Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
128130
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hereditary Paraganglioma/Pheochromocytoma Panel

Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia
United States
912
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Thyroid Cancer Panel

Invitae
United States
237
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Hyperparathyroidism Panel

Invitae
United States
95
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Multi-Cancer Panel

Invitae
United States
13980
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Invitae Multiple Endocrine Neoplasia Type 2 Test

Invitae
United States
61
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Inherited Cancer Panel

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University
United States
3349
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

RET Gene Sequencing and Deletion/Duplication Analysis

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
81
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 61 to 80 of 95

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.