Filters
Other countries
Results: 1 to 14 of 14
| Tests names and labs | Conditions | Genes, analytes, and microbes | Methods |
|---|---|---|---|
High-Resolution Rapid Microarray (CGH and SNP) Allele Diagnostics United States | 247 | 231 |
|
Rapid microarray (CGH and SNP) Allele Diagnostics United States | 247 | 231 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Xp11.22 microduplication syndrome, 300705 (X-linked non-syndromic intellectual disability) (440) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey | 1 | 1 |
|
Baylor Genetics United States | 2 | 1 |
|
HSD17B10 Sequence & Deletion/Duplication Analysis Baylor Genetics United States | 2 | 1 |
|
HSD17B10 Prenatal Sequence Analysis Baylor Genetics United States | 2 | 1 |
|
HSD17B10 Familial Mutation/Variant Analysis Baylor Genetics United States | 2 | 1 |
|
HSD17B10 Deletion/Duplication Analysis Baylor Genetics United States | 2 | 1 |
|
Baylor Genetics United States | 842 | 637 |
|
X-chromosome High Resolution microarray analysis Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center United States | 240 | 171 |
|
Mental retardation, X-linked type 17 (sequence analysis of HSD17B10 gene) CGC Genetics Unilabs Portugal | 1 | 1 |
|
Epileptic syndromes with epilepsy and intellectual disability panel Genome Diagnostics Laboratory University Medical Center Utrecht Netherlands | 74 | 50 |
|
Results: 1 to 14 of 14
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.