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Results: 1 to 20 of 26

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hypoparathyroidism, familial isolated, 146200, Autosomal dominant; FIH (Familial isolated hypoparathyroidism) (GCM2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Hypoparathyroidism, autosomal recessive, 146200, Autosomal dominant (Familial isolated hypoparathyroidism due to impaired PTH secretion) (PTH gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Hypoparathyroidism, autosomal dominant, 146200, Autosomal dominant (Familial isolated hypoparathyroidism due to impaired PTH secretion) (PTH gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Hypoparathyroidism Panel

PreventionGenetics, Part of Exact Sciences
United States
1515
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Familial Isolated Hypoparathyroidism via the GCM2 Gene

PreventionGenetics, Part of Exact Sciences
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Familial Isolated Hypoparathyroidism via the PTH Gene

PreventionGenetics, Part of Exact Sciences
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Female Infertility

Asper Biogene Asper Biogene LLC
Estonia
8564
  • C Sequence analysis of the entire coding region

Hyperparathyroidism NGS Panel

Fulgent Genetics
United States
166
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypothyroidism and Resistance to Thyroid Hormone NGS Panel

Fulgent Genetics
United States
4119
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

HYPOPARATHYROIDISM

Laboratorio de Genetica Clinica SL
Spain
14
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Familial Hypoparathyroidism , Sequencing PTH Gene

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

Familial Hypoparathyroidism , Sequencing CASR Gene

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

Single gene testing PTH

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

Hypoparathyroidism panel

Genetic Services Laboratory University of Chicago
United States
2117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

GCM2 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

Hypoparathyroidism

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Hypoparathyroidism

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Hypocalcemia, autosomal dominant

MedGene
Slovakia
11
  • C Sequence analysis of the entire coding region

Hypoparathyroidism, familial isolated 1

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: 1 to 20 of 26

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.