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                                       Details for article 4 of 19 found articles
 
 
  Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith–Magenis syndrome minimum deletion to ~650 kb
 
 
Title: Detection and delineation of an unusual 17p11.2 deletion by array-CGH and refinement of the Smith–Magenis syndrome minimum deletion to ~650 kb
Author: Schoumans, Jacqueline
Staaf, Johan
Jönsson, Göran
Rantala, Johanna
Zimmer, Kerstin Sars
Borg, Åke
Nordenskjöld, Magnus
Anderlid, Britt-Marie
Appeared in: European journal of medical genetics
Paging: Volume 48 (2005) nr. 3 pages 11 p.
Year: 2005
Contents:
Publisher: Elsevier SAS
Source file: Elektronische Wetenschappelijke Tijdschriften
 
 

                             Details for article 4 of 19 found articles
 
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