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Results: 1 to 20 of 323

Tests names and labsConditionsGenes, analytes, and microbesMethods

Rett/Atypical Rett Syndrome Panel

Genetic Services Laboratory University of Chicago
United States
19
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Rett syndrome, preserved speech variant, 312750, X-linked dominant; RTT (Rett syndrome) (MECP2 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Rett syndrome, 312750, X-linked dominant (Rett syndrome) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Rett syndrome, preserved speech variant, 312750, X-linked dominant; RTT (Rett syndrome) (MECP2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Rett syndrome, atypical, 312750, X-linked dominant (Atypical Rett syndrome) (MECP2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Rett syndrome, 312750, X-linked dominant (Rett syndrome) (MECP2 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Rett syndrome, preserved speech variant, 312750, X-linked dominant; RTT (Rett syndrome) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Rett syndrome, atypical, 312750, X-linked dominant (Atypical Rett syndrome) (MECP2 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Rett syndrome, atypical, 312750, X-linked dominant (Atypical Rett syndrome) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Rett syndrome, atypical, 312750, X-linked dominant (Atypical Rett syndrome) (Prenatal) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Rett syndrome, 312750, X-linked dominant (Rett syndrome) (MECP2 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Rett syndrome, 312750, X-linked dominant (Rett syndrome) (Prenatal) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Rett syndrome, preserved speech variant, 312750, X-linked dominant; RTT (Rett syndrome) (Prenatal) (MLPA)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • D Deletion/duplication analysis

Rett syndrome, congenital variant, 613454, Isolated cases (Atypical Rett syndrome) (FOXG1 gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Rett syndrome, congenital variant, 613454, Isolated cases (Atypical Rett syndrome) (FOXG1 gene) (Sequence Analysis-All Coding Exons) (Prenatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Rett and Rett-like syndrome (WES based NGS panel of 12 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
112
  • C Sequence analysis of the entire coding region

Rett Syndrome exon 4 hotspot mutations

Molecular Genetics Laboratory All India Institute of Medical Sciences Kalyani
India
21
  • X Mutation scanning of select exons

Rett syndrome (MECP2 gene)

Molecular Genetics and Cytogenetics, Clinical Laboratory Service RED DE SALUD UC CHRISTUS
Chile
11
  • C Sequence analysis of the entire coding region

MECP2 Gene Rett syndrome NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

MECP2 Gene Rett syndrome preserved speech variant NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

Results: 1 to 20 of 323

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.