CORE
🇺🇦
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
Additional file 1: Figure S1. of COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA
Authors
Adalbjorg Jonasdottir (3820867)
Agnar Helgason (49150)
+23 more
Asgeir Sigurdsson (245384)
Aslaug Jonasdottir (245327)
Asmundur Oddsson (4593238)
Brynjar Jensson (4593223)
Daniel Gudbjartsson (4593226)
Gerald Sulem (4593205)
Gisli Masson (418888)
Gudmundur Thorisson (4593220)
Gudny Arnadottir (4593211)
Gunnar Gudmundsson (3449237)
Hakon Jonsson (4593214)
Ingileif Jonsdottir (346412)
Jon Kristinsson (4593229)
Jona Saemundsdottir (4593217)
Kari Stefansson (26484)
Olafur Magnusson (524235)
Patrick Sulem (57401)
Ragnar Kristjansson (4593241)
Reynir Arngrimsson (4593232)
Sif Hansdottir (4593244)
Stefania Benonisdottir (4593208)
Unnur Thorsteinsdottir (49155)
Vigdis Petursdottir (4593235)
Publication date
Publisher
Doi
Cite
Abstract
Lung biopsy section from the index case (II-3) stained with hematoxylin and eosin. Mild interstitial lymphoid infiltrate and multiple foci of lymphoid hyperplasia. (DOCX 579Â kb
Similar works
Full text
Available Versions
FigShare
See this paper in CORE
Go to the repository landing page
Download from data provider
oai:figshare.com:article/56022...
Last time updated on 12/02/2018