Published in
Elsevier, Genetics in Medicine, 6(20), p. 645-654, 2018
DOI: 10.1038/gim.2017.162
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Clinical whole-exome sequencing for the diagnosis of rare disorders with congenital anomalies and/or intellectual disability: substantial interest of prospective annual reanalysis
Journal article published in 2017 by
Sophie Nambot,
Julien Thevenon,
Paul Kuentz,
Yannis Duffourd,
Emilie Tisserant,
Ange-Line Bruel,
Pierre Vabres,
Anne-Laure Mosca-Boidron,
Alice Masurel-Paulet,
Mathilde Lefebvre,
Frederic Tran Mau-Them 
,
Daphné Lehalle,
Salima El Chehadeh-Djebbar,
Nolwenn Jean-Marçais,
Christophe Philippe
and other authors.
,
Daphné Lehalle,
Salima El Chehadeh-Djebbar,
Nolwenn Jean-Marçais,
Christophe Philippe
and other authors.
This paper is made freely available by the publisher.
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