Skip to main content
Quest Diagnostics

Characterization of Molecular Diagnosis of Inherited Retinal Disease Within a Large Pediatric Cohort Undergoing Comprehensive Retinal Dystrophy Panel Next-Generation Sequencing Analysis

National Society of Genetic Councelors
41st Annual Conference

NSG 2022

Nashville, TN, November 16 - 20, 2022

Poster presentation: Characterization of molecular diagnosis of inherited retinal disease within a large pediatric cohort undergoing comprehensive retinal dystrophy panel next-generation sequencing analysis

Authors: Fuqua L, Navarro I, Gall K, Hathaway J, Alicia Scocchia, Kämpjärvi K, Känsäkoski J, von Nandelstadh P, Gandia M, Vattulainen-Collanus S, Mak K-Y, Mikk M-L, Sonia Casanovas S, Sarantaus L, Västinsalo H,Saarine I,  Tuupanen S, Koskenvuo J

Specialties: Genetics

Disclaimer:  One or more of the authors of this publication were employed at the time by Blueprint Genetics, a subsidiary of Quest Diagnostics.

Our company

Quest® is the brand name used for services offered by Quest Diagnostics Incorporated and its affiliated companies. Quest Diagnostics Incorporated and certain affiliates are CLIA certified laboratories that provide HIPAA covered services.  Other affiliates operated under the Quest® brand, such as Quest Consumer Inc., do not provide HIPAA covered services. 

 

Quest®, Quest Diagnostics®, any associated logos, and all associated Quest Diagnostics registered or unregistered trademarks are the property of Quest Diagnostics. All third-party marks—® and ™—are the property of their respective owners. © 2024 Quest Diagnostics Incorporated. All rights reserved. Image content features models and is intended for illustrative purposes only.