Clinical whole-exome sequencing for the diagnosis of rare disorders with congenital anomalies and/or intellectual disability: substantial interest of prospective annual reanalysis.
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| Description | scientific article published on 2 November 2017 |
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author: Pierre Vabres Antonio Vitobello Julien Thevenon Alice Masurel-Paulet Patrick Callier Paul Kuentz Ange-Line Bruel Christel Thauvin-Robinet |
| Publication date | November 2, 2017 |
| Language | English |
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