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Results: 1 to 6 of 6

Tests names and labsConditionsGenes, analytes, and microbesMethods

CDKN1C Gene, Full Gene Analysis

Mayo Clinic Laboratories Mayo Clinic
United States
31
  • C Sequence analysis of the entire coding region

EPISign Whole Genome Methylation Assay

Molecular Genetics Laboratory London Health Sciences Centre
Canada
191
  • M Methylation analysis

Russell-Silver Syndrome Methylation-Specific MLPA

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
11
  • M Methylation analysis

Beckwith-Wiedemann Syndrome (BWS) and Russell-Silver Syndrome (RSS) by Methylation-Specific MLPA

ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories
United States
21
  • M Methylation analysis

Chromosome 7 UPD Analysis

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
21
  • U Uniparental disomy study (UPD)

Silver-Russell syndrome (KCNQ1, H19, UPD7)

Center for Human Genetics Cliniques Universitaires Saint Luc
Belgium
12
  • M Methylation analysis

Results: 1 to 6 of 6

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.