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                                       Details for article 3 of 17 found articles
 
 
  A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome
 
 
Title: A Specific IFIH1 Gain-of-Function Mutation Causes Singleton-Merten Syndrome
Author: Rutsch, Frank
MacDougall, Mary
Lu, Changming
Buers, Insa
Mamaeva, Olga
Nitschke, Yvonne
Rice, Gillian I.
Erlandsen, Heidi
Kehl, Hans Gerd
Thiele, Holger
Nürnberg, Peter
Höhne, Wolfgang
Crow, Yanick J.
Feigenbaum, Annette
Hennekam, Raoul C.
Appeared in: The American journal of human genetics
Paging: Volume 96 (2015) nr. 2 pages 8 p.
Year: 2015
Contents:
Publisher: The American Society of Human Genetics
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 3 of 17 found articles
 
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