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Results: 41 to 54 of 54

Tests names and labsConditionsGenes, analytes, and microbesMethods

Hearing Loss Advanced Sequencing and CNV Evaluation

Athena Diagnostics Inc
United States
249184
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bartter Syndrome and related disorders , Panel Massive Sequencing (NGS) 22 Genes

Reference Laboratory Genetics
Spain
2122
  • C Sequence analysis of the entire coding region

BARTTER SYNDROME, ANTENATAL, TYPE 1

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Antenatal Bartter Syndrome Type 1, Sequencing SLC12A1 Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Bartter syndrome

Institute of Human Genetics Cologne University
Germany
106
  • C Sequence analysis of the entire coding region

SLC12A1 Gene Sequencing and Deletion/Duplication Analysis

DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Bartter syndrome type 1

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

SLC12A1 Single Gene

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

SLC12A1 DNA Sequencing Test

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

Hereditary Renal Tubular Disorders Evaluation

Athena Diagnostics Inc
United States
65
  • 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

Bartter Syndrome

Genetics Laboratory University of Oklahoma Health Sciences Center
United States
55
  • C Sequence analysis of the entire coding region

Antenatal Bartter Syndrome Type 1,SLC12A1

GGA - Galil Genetic Analysis
Israel
11
  • C Sequence analysis of the entire coding region

Bartter syndrome antenatal type 1

Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders
Germany
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 41 to 54 of 54

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.