Published in
Elsevier, Genetics in Medicine, 6(19), p. 667-675, 2017
DOI: 10.1038/gim.2016.163
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Detection of clinically relevant copy-number variants by exome sequencing in a large cohort of genetic disorders
Journal article published in 2016 by
Rolph Pfundt,
Marisol del Rosario 
,
Lisenka E. L. M. Vissers,
Michael P. Kwint,
Irene M. Janssen,
Nicole de Leeuw ,
Helger G. Yntema,
Marcel R. Nelen,
Dorien Lugtenberg,
Erik-Jan Kamsteeg,
Nienke Wieskamp,
Alexander P. A. Stegmann ,
Servi J. C. Stevens,
Richard J. T. Rodenburg ,
Annet Simons
and other authors.
,
Lisenka E. L. M. Vissers,
Michael P. Kwint,
Irene M. Janssen,
Nicole de Leeuw ,
Helger G. Yntema,
Marcel R. Nelen,
Dorien Lugtenberg,
Erik-Jan Kamsteeg,
Nienke Wieskamp,
Alexander P. A. Stegmann ,
Servi J. C. Stevens,
Richard J. T. Rodenburg ,
Annet Simons
and other authors.
This paper is made freely available by the publisher.
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