Digital Library
Close Browse articles from a journal
 
<< previous   
     Journal description
       All volumes of the corresponding journal
         All issues of the corresponding volume
           All articles of the corresponding issues
                                       Details for article 22 of 22 found articles
 
 
  Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia
 
 
Title: Zebrafish Ciliopathy Screen Plus Human Mutational Analysis Identifies C21orf59 and CCDC65 Defects as Causing Primary Ciliary Dyskinesia
Author: Austin-Tse, Christina
Halbritter, Jan
Zariwala, Maimoona A.
Gilberti, Renée M.
Gee, Heon Yung
Hellman, Nathan
Pathak, Narendra
Liu, Yan
Panizzi, Jennifer R.
Patel-King, Ramila S.
Tritschler, Douglas
Bower, Raqual
O’Toole, Eileen
Porath, Jonathan D.
Hurd, Toby W.
Chaki, Moumita
Diaz, Katrina A.
Kohl, Stefan
Lovric, Svjetlana
Hwang, Daw-Yang
Braun, Daniela A.
Schueler, Markus
Airik, Rannar
Otto, Edgar A.
Leigh, Margaret W.
Noone, Peadar G.
Carson, Johnny L.
Davis, Stephanie D.
Pittman, Jessica E.
Ferkol, Thomas W.
Atkinson, Jeffry J.
Olivier, Kenneth N.
Sagel, Scott D.
Dell, Sharon D.
Rosenfeld, Margaret
Milla, Carlos E.
Loges, Niki T.
Omran, Heymut
Porter, Mary E.
King, Stephen M.
Knowles, Michael R.
Drummond, Iain A.
Hildebrandt, Friedhelm
Appeared in: The American journal of human genetics
Paging: Volume 93 (2013) nr. 4 pages 15 p.
Year: 2013
Contents:
Publisher: The American Society of Human Genetics
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 22 of 22 found articles
 
<< previous   
 
 Koninklijke Bibliotheek - National Library of the Netherlands