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: Ahmet Kablan, Abdullah Sezer, Abdullatif Bakır, Elifcan Taşdelen, Firdevs Dinçsoy Bir, Haktan Bagis Erdem, Hanife Saat, Mustafa Tarık Alay, Abdulkerim Kolkıran, Melike Ataseven Kulali, Hakan Güneş
Format: Artículo Open Access
Published: Wiley 2025
Subjects:
Clinical Genetics
Online Access:https://onlinelibrary.wiley.com/doi/10.1111/cge.14740
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.14740

Similar Items

  • A founder deletion in ECM1 of 1163 bp causes lipoid proteinosis in the southeast region of Turkiye
    by: Elifcan Taşdelen, et al.
    Published: (2024)
  • Attenuated Form of Nijmegen Breakage Syndrome: Case Report of the Oldest Patient
    by: Sultan Kevser Gangal, et al.
    Published: (2025)
  • Presentation of hyperekplexia during the newborn period: Is there any additional treatment option to clonazepam?
    by: Dilek Cavusoglu, et al.
    Published: (2026)
  • Subwavelength resolution using the near field of quantum emitters
    by: Kolkiran, Aziz
    Published: (2024)
  • The Effect of Mandala Design Training on Perceptual Skills of Children With Specific Learning Disorder
    by: Elifcan Cesur
    Published: (2025)

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