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gim.2017.162
gim.2017.162
https://scigraph.springernature.com/pub.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.
P2888
Q45951588-5111C08F-D45E-456C-B0BF-AEE4003F5D70
P2888
gim.2017.162
https://scigraph.springernature.com/pub.10.1038/gim.2017.162