Filters

See more specimen types...

Other countries

Results: 1 to 20 of 22

Tests names and labsConditionsGenes and analytesMethods

AllNeuro panel

Centogene AG - the Rare Disease Company
Germany
6021038
  • C Sequence analysis of the entire coding region

Rapid microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • H Detection of homozygosity
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Speech-language disorder type 1

Centogene AG - the Rare Disease Company
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Speech-Language Disorder 1

(AC) Atlanta Center: Medical Neurogenetics, LLC.
United States
11
  • C Sequence analysis of the entire coding region

TruGenome Predisposition Screen (Whole Genome Sequencing)

Illumina Clinical Services Laboratory Illumina
United States
15391578
  • C Sequence analysis of the entire coding region

Rett, Syndrome

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
2018
  • C Sequence analysis of the entire coding region

Autism

GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases
Spain
2528
  • C Sequence analysis of the entire coding region

Speech-Language Disorder 1, FOXP2

Center for Human Genetics, Inc
United States
11
  • C Sequence analysis of the entire coding region

IDNext

Ambry Genetics
United States
12140
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Neurodevelopment-Expanded

Ambry Genetics
United States
105196
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Autsim Panel

Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health and Science University
United States
1107
  • C Sequence analysis of the entire coding region

FOXP2

MVZ Dortmund Dr. Eberhard and Partner
Germany
11
  • C Sequence analysis of the entire coding region

Autism Spectrum Disorders Panel

ApolloGen, Inc.
United States
1101
  • A Analyte

Syndromic Autism Panel

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
183
  • C Sequence analysis of the entire coding region

FOXP2

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

Autism Panel: Tier 2

Emory Genetics Laboratory Emory University
United States
10360
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Speech-language disorder 1 (sequence analysis of FOXP2 gene)

CGC Genetics
Portugal
11
  • C Sequence analysis of the entire coding region

Autism NGS Panel

Fulgent Clinical Diagnostics Lab Fulgent Diagnostics
United States
177100
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Speech-Language Disorder 1: FOXP2 Gene Deletion/Duplication

Emory Genetics Laboratory Emory University
United States
11
  • D Deletion/duplication analysis

Speech-Language Disorder 1: FOXP2 Full Gene Sequencing

Emory Genetics Laboratory Emory University
United States
11
  • C Sequence analysis of the entire coding region

Results: 1 to 20 of 22

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.