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                                       Details for article 8 of 17 found articles
 
 
  PGD in the lab for triplet repeat diseases — myotonic dystrophy, Huntington's disease and Fragile-X syndrome
 
 
Title: PGD in the lab for triplet repeat diseases — myotonic dystrophy, Huntington's disease and Fragile-X syndrome
Author: Sermon, Karen
Seneca, Sara
De Rycke, Martine
Goossens, Veerle
Van de Velde, Hilde
De Vos, Anick
Platteau, Peter
Lissens, Willy
Van Steirteghem, André
Liebaers, Inge
Appeared in: Molecular and cellular endocrinology
Paging: Volume 183 (2001) nr. S1 pages 9 p.
Year: 2001
Contents:
Publisher: Elsevier Science Ireland Ltd
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 8 of 17 found articles
 
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