U.S. flag

An official website of the United States government

Filters

See more specimen types...

Other countries

Results: 21 to 40 of 40

Tests names and labsConditionsGenes, analytes, and microbesMethods

Central skeletal dysplasias panel. NGS panel of 111 genes.

Genologica Medica
Spain
258111
  • C Sequence analysis of the entire coding region

Meier-Gorlin syndrome panel. 6-gene NGS panel.

Genologica Medica
Spain
66
  • C Sequence analysis of the entire coding region

3M syndrome / primordial dwarfism panel. NGS panel of 24 genes.

Genologica Medica
Spain
3324
  • C Sequence analysis of the entire coding region

ORC6 gene sequencing

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • C Sequence analysis of the entire coding region

Microcephaly Panel

CNH Molecular Diagnostics Laboratory Childrens National Hospital
United States
6748
  • C Sequence analysis of the entire coding region

Meier-Gorlin syndrome: Full gene sequencing panel

CEN4GEN Institute for Genomics and Molecular Diagnostics
Canada
88
  • C Sequence analysis of the entire coding region

3-M Syndrome NGS Panel

Fulgent Genetics
United States
2116
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Meier-Gorlin Syndrome , Panel Massive Sequencing (NGS) 5 Genes

Reference Laboratory Genetics
Spain
55
  • C Sequence analysis of the entire coding region

Primordial Dwarfism and Related Disorders , Panel Massive Sequencing (NGS) 12 Genes

Reference Laboratory Genetics
Spain
1212
  • C Sequence analysis of the entire coding region

Brain malformations

Asper Biogene Asper Biogene LLC
Estonia
318252
  • C Sequence analysis of the entire coding region

ORC6 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

Single gene testing ORC6

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

Meier-Gorlin syndrome

Bicknell laboratory University of Otago
New Zealand
87
  • C Sequence analysis of the entire coding region

Selected Genetic Syndromes with skeletal involvement Panel

CeGaT GmbH
Germany
3642
  • C Sequence analysis of the entire coding region

Microcephaly

Asper Biogene Asper Biogene LLC
Estonia
11196
  • C Sequence analysis of the entire coding region

ORC6 Single Gene

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

Meier-Gorlin Syndrome NGS Panel

Fulgent Genetics
United States
55
  • 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

Primordial Dwarfism NGS Panel

Fulgent Genetics
United States
1612
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Meier-Gorlin Syndrome 3

Molecular Diagnostics Lab Nemours Children's Health, Delaware
United States
11
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 40

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.