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| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
Labcorp Genetics (formerly Invitae) LabCorp United States | 466 | 297 |
|
Invitae Cornelia de Lange Syndrome and Related Disorders Panel Labcorp Genetics (formerly Invitae) LabCorp United States | 44 | 31 |
|
X-Linked Intellectual Disability Panel PreventionGenetics, part of Exact Sciences United States | 191 | 141 |
|
Craniofacial Malformations Panel PreventionGenetics, part of Exact Sciences United States | 33 | 19 |
|
Cornelia de Lange Syndrome Panel PreventionGenetics, part of Exact Sciences United States | 8 | 8 |
|
Cornelia de Lange Syndrome via the HDAC8 Gene PreventionGenetics, part of Exact Sciences United States | 2 | 1 |
|
X-chromosome High Resolution microarray analysis Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center United States | 240 | 171 |
|
Cornelia de Lange syndrome 5 (sequence analysis of HDAC8 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Cornelia de Lange syndrome: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada | 5 | 5 |
|
Intellectual Disability X-linked Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 136 | 90 |
|
Intellectual Disability & Autism Spectrum Disorders Panel CNH Molecular Diagnostics Laboratory Childrens National Hospital United States | 210 | 139 |
|
Al Jalila Children’s Genomics Center Al Jalila Childrens Speciality Hospital United Arab Emirates | 10 | 10 |
|
CORNELIA DE LANGE SYNDROME (X-LINKED) Laboratorio de Genetica Clinica SL Spain | 2 | 2 |
|
Cornelia de Lange Syndrome Panel Genomic Diagnostic Laboratory, Division of Genomic Diagnostics Children's Hospital of Philadelphia United States | 10 | 10 |
|
PreSeek™ Non-invasive Prenatal Gene Sequencing Screen Baylor Genetics United States | 48 | 30 |
|
CeGaT GmbH Germany | 2 | 1 |
|
Cohesinopathies (Cornelia de Lange Syndrome) MGZ Medical Genetics Center Germany | 5 | 5 |
|
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.