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                                       Details for article 13 of 19 found articles
 
 
  NR2F1 Mutations Cause Optic Atrophy with Intellectual Disability
 
 
Title: NR2F1 Mutations Cause Optic Atrophy with Intellectual Disability
Author: Bosch, Daniëlle G.M.
Boonstra, F. Nienke
Gonzaga-Jauregui, Claudia
Xu, Mafei
de Ligt, Joep
Jhangiani, Shalini
Wiszniewski, Wojciech
Muzny, Donna M.
Yntema, Helger G.
Pfundt, Rolph
Vissers, Lisenka E.L.M.
Spruijt, Liesbeth
Blokland, Ellen A.W.
Chen, Chun-An
Lewis, Richard A.
Tsai, Sophia Y.
Gibbs, Richard A.
Tsai, Ming-Jer
Lupski, James R.
Zoghbi, Huda Y.
Cremers, Frans P.M.
de Vries, Bert B.A.
Schaaf, Christian P.
Appeared in: The American journal of human genetics
Paging: Volume 94 (2014) nr. 2 pages 7 p.
Year: 2014
Contents:
Publisher: The American Society of Human Genetics
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 13 of 19 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands