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Results: 41 to 56 of 56

Tests names and labsConditionsGenes, analytes, and microbesMethods

Complete PKD Evaluation

Athena Diagnostics
United States
22
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PKD1 DNA Sequencing Test

Athena Diagnostics
United States
11
  • C Sequence analysis of the entire coding region

PKD1 DNA Sequencing and Deletion Evaluation

Athena Diagnostics
United States
12
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Nephrology Endocrinology and Electrolytes - panels

MGZ Medical Genetics Center
Germany
5117
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Autosomal dominant polycystic kidney disease type 1

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

Polycystic kidney disease

Institute of Human Genetics Cologne University
Germany
109
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PKD2 - Polycystic Kidney Disease

MGZ Medical Genetics Center
Germany
21
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Polycystic kidney disease, adult type I (MLPA)

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • D Deletion/duplication analysis

Polycystic kidney disease, adult type I

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • C Sequence analysis of the entire coding region

Polycystic kidney disease, adult type I

MVZ Dr. Eberhard & Partner Dortmund
Germany
11
  • C Sequence analysis of the entire coding region

PKD1 Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Polycystic Kidney Disease NGS Panel

Fulgent Genetics
United States
46
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

PKDx® Familial Mutation Evaluation

Athena Diagnostics
United States
22
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Congenital Hepatic Fibrosis NGS Panel

Fulgent Genetics
United States
4734
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Polycystic Kidney Disease 1, Autosomal Dominant

Molecular Genetics, Function and Therapy The Cyprus Institute of Neurology and Genetics
Cyprus
11
  • L Linkage analysis

Results: 41 to 56 of 56

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.