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                                       Details for article 7 of 130 found articles
 
 
  A novel mutation in the MAGEL2 gene in a patient with arthrogryposis, severe global developmental delay and autistic features
 
 
Title: A novel mutation in the MAGEL2 gene in a patient with arthrogryposis, severe global developmental delay and autistic features
Author: Ardicli, D.
Zaharieva, I.
Phadke, R.
Scoto, M.C.
Borrel, L.M.
Laurie, S.
Agullo, S.B.
Sarkozy, A.
Muntoni, F.
Appeared in: Neuromuscular disorders
Paging: Volume 28 (2018) nr. S1 pages S36-S37
Year: 2018
Contents:
Publisher: Elsevier B.V.
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 7 of 130 found articles
 
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 Koninklijke Bibliotheek - National Library of the Netherlands