Skip to content
VuFind
  • Login
    • English
    • Deutsch
    • Español
    • Français
    • Italiano
Advanced
  • Cite this
  • Text this
  • Email this
  • Print
  • Export Record
    • Export to RefWorks
    • Export to EndNoteWeb
    • Export to EndNote
  • Save to List
  • Permanent link
Cover Image

Saved in:
Bibliographic Details
Main Authors: Elena Zinina, Maria Bulakh, Alena Chukhrova, Oksana Ryzhkova, Olga Shchagina, Aleksander Polyakov
Format: Artículo Open Access
Published: Wiley 2025
Subjects:
Clinical Genetics
Online Access:https://onlinelibrary.wiley.com/doi/10.1111/cge.14747
Tags: Add Tag
No Tags, Be the first to tag this record!
  • Holdings
  • Description
  • Table of Contents
  • Comments
  • Similar Items
  • Staff View

Internet

https://onlinelibrary.wiley.com/doi/10.1111/cge.14747

Similar Items

  • Clinical and Genetic Analysis of Digenic Muscular Dystrophy due to SRPK3 and TTN Variants in Two Siblings
    by: Inna Sharkova, et al.
    Published: (2024)
  • The first case of a point pathogenic variant in the RREB1 gene in Noonan‐like Rasopathy
    by: Olga Shatokhina, et al.
    Published: (2024)
  • Rare Cause 5q SMA : Molecular Genetic and Clinical Analyses of Intragenic Subtle Variants in the SMN Locus
    by: Kristina Mikhalchuk, et al.
    Published: (2025)
  • The Role of Whole‐Exome Sequencing and Methylation Analysis in Untangling Complex Facioscapulo‐Humeral Muscular Dystrophy Cases
    by: Francesca Torri, et al.
    Published: (2025)
  • Genetic Landscape of Hearing Loss in Brazilian Patients Reveals Population‐Specific Variants and Clinical Correlations
    by: Stella Diogo‐Cavassana, et al.
    Published: (2026)

Search Options

  • Search History
  • Advanced Search

Find More

  • Browse the Catalog
  • Browse Alphabetically
  • Explore Channels
  • Course Reserves
  • New Items

Need Help?

  • Search Tips
  • Ask a Librarian
  • FAQs