Novel UBR1 gene mutation in a patient with typical phenotype of Johanson–Blizzard syndrome

Published 2010 View Full Article

  1. Home
  2. Publications
  3. Publication Search
  4. Publication Details
Title
Novel UBR1 gene mutation in a patient with typical phenotype of Johanson–Blizzard syndrome
Authors
Keywords
-
Journal
EUROPEAN JOURNAL OF PEDIATRICS
Volume 170, Issue 2, Pages 233-235
Publisher
Springer Nature
Online
2010-06-16
DOI
10.1007/s00431-010-1239-y

Ask authors/readers for more resources

Protocol

Community support

Reagent

Community support

Reprint

Contact the author

Publish scientific posters with Peeref

Peeref publishes scientific posters from all research disciplines. Our Diamond Open Access policy means free access to content and no publication fees for authors.

Learn More

Ask a Question. Answer a Question.

Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.

Get Started
Webinars Posters Questions Hubs Funding Journals Articles Connect Collections Reviewers About Us FAQs Mobile App Privacy Policy Terms of Use
© Peeref 2019-2024. All rights reserved.