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GIM.2017.162
GIM.2017.162
http://dx.doi.org/10.1038/GIM.2017.162
Clinical whole-exome sequencing for the diagnosis of rare disorders with congenital anomalies and/or intellectual disability: substantial interest of prospective annual reanalysis.
P356
Q45951588-D98720C3-899A-43B9-A1EB-83763024A7F9
P356
GIM.2017.162
http://dx.doi.org/10.1038/GIM.2017.162