U.S. flag

An official website of the United States government

Filters

See more specimen types...
See more states

Other countries

See more countries

Results: 21 to 40 of 128

Tests names and labsConditionsGenes, analytes, and microbesMethods

Diabetes and Obesity Panel

Centogene AG - the Rare Disease Company
Germany
247262
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region
  • T Targeted variant analysis

Invitae Neurodevelopmental Disorders Panel

Invitae
United States
404241
  • D Deletion/duplication analysis

Invitae Monogenic Obesity Panel

Invitae
United States
9268
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Prader-Willi/Angelman Syndrome DNA Methylation

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
21
  • M Methylation analysis

Prader-Willi syndrome, 176270, Isolated cases (Prader-Willi syndrome) (Prenatal) (MLPA)

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

Prader-Willi syndrome, 176270, Isolated cases (Prader-Willi syndrome) (MLPA)

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

Prader-Willi syndrome, 176270, Isolated cases; PWS (Prader-Willi syndrome) (MLPA)

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

Prader-Willi syndrome, 176270, Isolated cases (Prader-Willi syndrome) (SNRPN 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

Prader-Willi syndrome, 176270, Isolated cases; PWS (Prader-Willi syndrome) (NDN 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

Prader-Willi syndrome, 176270, Isolated cases; PWS (Prader-Willi syndrome) (Prenatal) (MLPA)

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

Prader-Willi syndrome, 176270, Isolated cases (Prader-Willi syndrome) (SNRPN 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

Prader-Willi syndrome, 176270, Isolated cases; PWS (Prader-Willi syndrome) (NDN 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

Prader-Willi or Angelman Syndrome Analysis

IU Genetic Testing Laboratories Indiana University School of Medicine
United States
22
  • M Methylation analysis

qChip 180

Quantitative Genomic Medicine Laboratories, SL
Spain
184162
  • D Deletion/duplication analysis

Prader-Willi syndrome

Genetics Service Unit National Institute of Biomedical Genomics
India
11
  • D Deletion/duplication analysis

Prader – Willi syndrome Methylation specific MLPA

Genetics Service Unit National Institute of Biomedical Genomics
India
11
  • M Methylation analysis

Methylation study for Prader Willi and Angelman Syndrome

Institute of Human Genetics Foundation for Research in Genetics and Endocrinology
India
21
  • M Methylation analysis

QNatal Advanced

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
1513
  • C Sequence analysis of the entire coding region

Constitutional Chromosomal Microarray Analysis

Clinical Genomics Laboratory Laboratory for Precision Diagnostics, University of Washington
United States
261
  • D Deletion/duplication analysis

Prader-Willi syndrome FISH

Cytogenetics Laboratory University Of Washington
United States
11
  • M FISH-metaphase

Results: 21 to 40 of 128

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.