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Results: 1 to 11 of 11

Tests names and labsConditionsGenes, analytes, and microbesMethods

Chromosome 15q11.2 deletion syndrome, 615656, Autosomal dominant (15q11.2 microdeletion syndrome) (440)

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

Chromosome 15q11.2 deletion syndrome, 615656, Autosomal dominant (15q11.2 microdeletion syndrome) (Prenatal) (440)

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

Cardio PGx Panel

Dynamic DNA Laboratories, LLC
United States
166
  • D Deletion/duplication analysis
  • T Targeted variant analysis

Comprehensive PGx Panel

Dynamic DNA Laboratories, LLC
United States
12518
  • D Deletion/duplication analysis
  • T Targeted variant analysis

High-Resolution Rapid Microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • D Deletion/duplication analysis
  • H Detection of homozygosity

aCGH study for cryptic quantitative genomic imbalances

Institute of Human Genetics Foundation for Research in Genetics and Endocrinology
India
9024
  • D Deletion/duplication analysis

Rxight Pharmacogenetics Program

MD Labs
United States
628
  • T Targeted variant analysis

Rapid microarray (CGH and SNP)

Allele Diagnostics
United States
247231
  • D Deletion/duplication analysis
  • H Detection of homozygosity

Invitae NIPS for Singleton Pregnancies (chromosomes 13, 18, 21)

Labcorp Genetics (formerly Invitae) LabCorp
United States
1111
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Microarray Testing

Cytogenetics Laboratory SUNY Upstate Medical University
United States
1141
  • F Fluorescence in situ hybridization (FISH)

Non-invasive Prenatal Screen with Microdeletions

PathGroup
United States
1110
  • T Targeted variant analysis

Results: 1 to 11 of 11

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