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Results: 21 to 39 of 39

Tests names and labsConditionsGenes, analytes, and microbesMethods

Inherited Metabolic Disorders Panel

Dhiti Omics Technologies Private Ltd
India
376317
  • C Sequence analysis of the entire coding region

Nephrolithiasis panel. 35-gene NGS panel.

Genologica Medica
Spain
6035
  • C Sequence analysis of the entire coding region

Osteogenesis imperfecta panel. 28-gene NGS panel.

Genologica Medica
Spain
4827
  • C Sequence analysis of the entire coding region

Skeletal disease dysplasia panel with abnormal mineralization. 32-gene NGS panel.

Genologica Medica
Spain
6032
  • C Sequence analysis of the entire coding region

Hypophosphatemic rickets panel. NGS panel of 13 genes.

Genologica Medica
Spain
2513
  • C Sequence analysis of the entire coding region

Skeletal diseases. NGS panel of 169 genes.

Genologica Medica
Spain
373169
  • C Sequence analysis of the entire coding region

Osteogenesis Imperfecta and Low Bone Density Panel, Sequencing

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
3426
  • C Sequence analysis of the entire coding region

Hypophosphatasia and Hypophosphatemic Rickets Panel

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
1110
  • C Sequence analysis of the entire coding region

Osteogenesis Imperfecta and Decreased Bone Density NGS Panel

Fulgent Genetics
United States
11132
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypophosphatemic Rickets NGS Panel

Fulgent Genetics
United States
3110
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Abnormal Mineralization NGS Panel

Fulgent Genetics
United States
7730
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Abnormal Mineralization , Panel Massive Sequencing (NGS) 28 Genes

Reference Laboratory Genetics
Spain
3428
  • C Sequence analysis of the entire coding region

Skeletal dysplasia with abnormal mineralization Panel

CeGaT GmbH
Germany
1416
  • C Sequence analysis of the entire coding region

Hypophosphatemic rickets Panel

CeGaT GmbH
Germany
711
  • C Sequence analysis of the entire coding region

CLCN5 Single Gene

Fulgent Genetics
United States
41
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Skeletal Dysplasias NGS Panel

Fulgent Genetics
United States
543178
  • 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

Nuclear-Mito NGS Panel

Fulgent Genetics
United States
1103676
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Dent Disease (Type 1, Type 2) Genetic Testing

Rare Kidney Stone Consortium And The Mayo Clinic Hyperoxaluria Center Mayo Clinic
United States
32
  • C Sequence analysis of the entire coding region

Results: 21 to 39 of 39

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.