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Results: 21 to 40 of 47

Tests names and labsConditionsGenes, analytes, and microbesMethods

Wolf-Hirschhorn syndrome

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

Constitutional Chromosomal Microarray Analysis

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

Wolf-Hirschhorn syndrome FISH

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

Wolf-Hirschhorn Syndrome

Genetics Laboratory Shodair Children's Hospital
United States
11
  • M FISH-metaphase

FISH, Wolf-Hirschhorn

Quest Diagnostics Nichols Institute San Juan Capistrano
United States
11
  • M FISH-metaphase

FISH, Wolf-Hirschhorn

Quest Diagnostics Nichols Institute Chantilly
United States
11
  • M FISH-metaphase

Detection by FISH of Wolf-Hirschhorn syndrome

CGC Genetics Unilabs
Portugal
11
  • F Fluorescence in situ hybridization (FISH)

NIPT extended

CIBIC S.A.
Argentina
1112
  • D Deletion/duplication analysis

NIPT in POC

CIBIC S.A.
Argentina
1112
  • D Deletion/duplication analysis

NIPT Basic

CIBIC S.A.
Argentina
114
  • D Deletion/duplication analysis

EpiSign Variant

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
341
  • M Methylation analysis

Wolf-Hirschhorn Syndrome (FISH)

Duzen Laboratories Duzen BBAGUAS
Turkey
11
  • M FISH-metaphase

Microdeletion FISH - Wolf-Hirschhorn WHSC (4516.3)

Genetiks Genetic Diagnosis Center Genetic Diseases Evaluation Center
Turkey
11
  • M FISH-metaphase

Microdeletion FISH

Integrated Genetics Cytogenetics and Biochemistry Laboratory
United States
101
  • M FISH-metaphase

EpiSign Complete

Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center
United States
341
  • M Methylation analysis

Non-invasive Prenatal Screen with Microdeletions

PathGroup
United States
1110
  • T Targeted variant analysis

MaterniT GENOME

Integrated Genetics – Sequenom
United States
231
  • T Targeted variant analysis

Prequel Prenatal Screen

Myriad Genetics, Inc.
United States
1310
  • C Sequence analysis of the entire coding region

180K CGH+SNP microarray analysis

Pittsburgh Cytogenetics Laboratory University of Pittsburgh Medical Center
United States
2311
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Single gene testing WHSC1

CeGaT GmbH
Germany
11
  • C Sequence analysis of the entire coding region

Results: 21 to 40 of 47

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.