CORE
🇺🇦Â
 make metadata, not war
Services
Services overview
Explore all CORE services
Access to raw data
API
Dataset
FastSync
Content discovery
Recommender
Discovery
OAI identifiers
OAI Resolver
Managing content
Dashboard
Bespoke contracts
Consultancy services
Support us
Support us
Membership
Sponsorship
Community governance
Advisory Board
Board of supporters
Research network
About
About us
Our mission
Team
Blog
FAQs
Contact us
A mutation in DOP1B identified as a probable cause for autosomal recessive Peters anomaly in a consanguineous family
Authors
Hamid Ahmadieh
Afagh Alavi
+8Â more
Alireza Baradaran-Rafii
Ensieh Darbari
Elahe Elahi
Sepehr Feizi
Seyed Bagher Hosseini
Shohreh Issazadeh-Navikas
Mozhgan Rezaei Kanavi
Davood Zare-Abdollahi
Publication date
1 January 2020
Publisher
Abstract
Abstract is not available.
Similar works
Full text
Available Versions
Copenhagen University Research Information System
See this paper in CORE
Go to the repository landing page
Download from data provider
oai:pure.atira.dk:publications...
Last time updated on 21/12/2020
