Digital Library
Close Browse articles from a journal
 
   next >>
     Journal description
       All volumes of the corresponding journal
         All issues of the corresponding volume
           All articles of the corresponding issues
                                       Details for article 1 of 26 found articles
 
 
  ARCN1 Mutations Cause a Recognizable Craniofacial Syndrome Due to COPI-Mediated Transport Defects
 
 
Title: ARCN1 Mutations Cause a Recognizable Craniofacial Syndrome Due to COPI-Mediated Transport Defects
Author: Izumi, Kosuke
Brett, Maggie
Nishi, Eriko
Drunat, Séverine
Tan, Ee-Shien
Fujiki, Katsunori
Lebon, Sophie
Cham, Breana
Masuda, Koji
Arakawa, Michiko
Jacquinet, Adeline
Yamazumi, Yusuke
Chen, Shu-Ting
Verloes, Alain
Okada, Yuki
Katou, Yuki
Nakamura, Tomohiko
Akiyama, Tetsu
Gressens, Pierre
Foo, Roger
Passemard, Sandrine
Tan, Ene-Choo
El Ghouzzi, Vincent
Shirahige, Katsuhiko
Appeared in: The American journal of human genetics
Paging: Volume 99 (2016) nr. 2 pages 9 p.
Year: 2016
Contents:
Publisher: American Society of Human Genetics
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 1 of 26 found articles
 
   next >>
 
 Koninklijke Bibliotheek - National Library of the Netherlands